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Ad Tape & Label

ATL (Ad Tape & Label Co) has a modern manufacturing plant located in Menomonee Falls, Wisconsin. We specialize in contract manufacturing of printed die-cut components and disposable medical devices. Our custom label capabilities include multi-panel booklet labels, as well as direct mail, industrial, product identification and security labels. - contract manufacturing

Prototyping and Engineering, Medical Die Cutting, Flexographic Label Printing, Contract Manufacturing, Custom Packaging & Pouching, Disposable Medical Devices, Medical Device Labels, Medical Tapes & Foams, Disposable Eye Patches, Island Placement, Industrial Labels, Product Labels, Instant Redeemable Coupons, Custom Scratch-Off Labels, Booklet Labels, Security Labels, & more.

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ATL To Highlight Medical Device Labels At MD&M East 2016 ATL-Exhibits-Medical-Device-Labels-at-MDM-East-2016 : ATL to Highlight Medical Device Labels at MD&M East 2016 (PDF)
Design & Manufacturing New England ATL-Medical-Device-Manufacturer-Boston-Show-May-2015 : Design & Manufacturing New England (PDF)
FMEA (Failure Modes & Effects Analysis) - Quality System 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : FMEA (Failure Modes & Effects Analysis) (PDF)
DOE (Design Of Experiments) - Quality System 006 Design Of Experiments Flow Chart 05-20-2015 WT : DOE (Design of Experiments) (PDF)
ATLMedicalSellSheet2014LOW - Medical Industry Sell Sheet ATLMedicalSellSheet2014LOW : medical industry sell sheet (PDF)
Quality System Atl-new-product-development-planning : Quality System (PDF)
ATLDirectMailSellSheet2014LOW - Direct Mail Sell Sheet ATLDirectMailSellSheet2014LOW : direct mail sell sheet (PDF)
ATL-Security-Sell-Sheet - Security Industry Sell Sheet ATL-Security-Sell-Sheet : security industry sell sheet (PDF)
43-quality-validation-steps - Quality System 43-quality-validation-steps : Quality System (PDF)
Medical Devices Sell Sheet - Disposable Medical Devices 3M-Medical-Device-Brochure-New : medical devices sell sheet (PDF)
Blog 011 What Is Systems Validation Protocol WT : Blog (PDF)
Tapes & Foams Sell Sheet - Medical Tapes & Foams 3M MedSpec Silicone-Adhesive-WhitePaper Feb12 : tapes & foams sell sheet (PDF)
Blog 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : Blog (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis - Blog 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Blog 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : Blog (PDF)
Risk Analysis - Blog 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
Process Capability - Blog 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : Process Capability (PDF)
Blog 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : Blog (PDF)
ATLSpecialtySellSheet2014LOW - Booklet Labels Sell Sheet ATLSpecialtySellSheet2014LOW : booklet labels sell sheet (PDF)
ATL-Security-Sell-Sheet - Security Industry Sell Sheet - Security Labels ATL-Security-Sell-Sheet : security industry sell sheet (PDF)
Nistaa Inc. Debuts New Disposable Medical Device - White Papers Nistaa-disposable-medical-device-launch : Nistaa Inc. Debuts New Disposable Medical Device (PDF)
ATL-Top-Ten-Vendor-Tips1 - OEM Medical Device Outsourcing Top Ten Tips + 1 - White Papers ATL-Top-Ten-Vendor-Tips1 : OEM Medical Device Outsourcing Top Ten Tips 1 (PDF)
ATL FDA Medical Device Quality White Paper - White Papers ATL FDA CGMP Medical Device Quality Whitepaper : ATL FDA Medical Device Quality White Paper (PDF)
APQP: Advanced Product Quality Planning - White Papers 001 Advanced Product Quality Planning APQP 05-20-2015 WT : APQP: Advanced Product Quality Planning  (PDF)
3M Medical Device Material Options - Resource Center 3M-Medical-Device-Brochure-New : 3M Medical Device Material Options (PDF)
ATL New Product Development - White Papers 002 New Product Development Flow Chart 05-22-2015 WT : ATL New Product Development (PDF)
ISO-14971 Risk Analysis - White Papers 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : ISO-14971 Risk Analysis (PDF)
What Is FMEA (Failure Modes & Effects Analysis)? - White Papers 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : What is FMEA (Failure Modes & Effects Analysis)? (PDF)
How To Do A Process FMEA - White Papers 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA (PDF)
3M Silicone Pressure Sensitive Tapes - Resource Center -3M-MedSpec-Silicone-PSA-Platform-Flyer Jan12 : 3M Silicone Pressure Sensitive Tapes (PDF)
D.O.E. - Design Of Experiments - White Papers 006 Design Of Experiments Flow Chart 05-20-2015 WT : D.O.E. - Design of Experiments (PDF)
FDA PQ - White Papers 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : FDA PQ (PDF)
ATL-Security-Sell-Sheet - Security Label Systems - Resource Center ATL-Security-Sell-Sheet : Security Label Systems (PDF)
How To Determine Process Capability - White Papers 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : How to Determine Process Capability (PDF)
ATLDirectMailSellSheet2014LOW - Direct Mail & Specialty Labels - Resource Center ATLDirectMailSellSheet2014LOW : Direct Mail & Specialty Labels (PDF)
ATLMedicalSellSheet2014LOW - Medical Die Cutting - Resource Center ATLMedicalSellSheet2014LOW : Medical Die Cutting (PDF)
ATLSpecialtySellSheet2014LOW - Booklet & Extended Content Labels - Resource Center ATLSpecialtySellSheet2014LOW : Booklet & Extended Content Labels (PDF)
Six-Sigma Projects (Disposable Medical Devices) - White Papers 010 Six-Sigma Explained With Fishbone Example Logo : Six-Sigma Projects (Disposable Medical Devices) (PDF)
What Is Validation Or Systems Validation Protocol? - White Papers 011 What Is Systems Validation Protocol WT : What Is Validation Or Systems Validation Protocol? (PDF)
Systems Validation Protocol Methods At ATL - Resource Center 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : Systems Validation Protocol Methods at ATL (PDF)
Disposable Medical Devices 011 What Is Systems Validation Protocol WT : disposable medical devices (PDF)
Disposable Medical Devices 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : disposable medical devices (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis - Disposable Medical Devices 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Disposable Medical Devices 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : disposable medical devices (PDF)
Risk Analysis - Disposable Medical Devices 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
Process Capability - Disposable Medical Devices 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : Process Capability (PDF)
Disposable Medical Devices 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : disposable medical devices (PDF)
Read Our White Paper - Helping A Client Launch A New Disposable Medical Device Nistaa-disposable-medical-device-launch : Read our white paper (PDF)
Systems Validation Protocol Methods For Disposable Medical Devices 011 What Is Systems Validation Protocol WT : Systems Validation Protocol Methods for Disposable Medical Devices (PDF)
Systems Validation Protocol 011 What Is Systems Validation Protocol WT : systems validation protocol (PDF)
Don Dobert 011 What Is Systems Validation Protocol WT : Don Dobert (PDF)
Don Dobert 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : Don Dobert (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis - Don Dobert 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Don Dobert 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : Don Dobert (PDF)
Risk Analysis - Don Dobert 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
President's Corner 011 What Is Systems Validation Protocol WT : President's Corner (PDF)
President's Corner 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : President's Corner (PDF)
Process Capability - Don Dobert 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : Process Capability (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis - President's Corner 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Don Dobert 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : Don Dobert (PDF)
President's Corner 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : President's Corner (PDF)
Risk Analysis - President's Corner 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
Process Capability - President's Corner 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : Process Capability (PDF)
Quality Management 011 What Is Systems Validation Protocol WT : quality management (PDF)
Quality Management 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : quality management (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis - Quality Management 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Quality Management 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : quality management (PDF)
Risk Analysis - Quality Management 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
Process Capability - Quality Management 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : Process Capability (PDF)
Quality Management 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : quality management (PDF)
Control Plans For Disposable Medical Devices 007 What Is A Control Plan Or FDA Performance Qualification PQ WT(1) : Control Plans for Disposable Medical Devices (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis - Process FMEA For Disposable Medical Devices 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Process FMEA For Disposable Medical Devices 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : Process FMEA for Disposable Medical Devices (PDF)
How To Do A Process FMEA For Medical Devices After ISO-17791 Risk Analysis 005 How To Do A Process FMEA For Medical Devices After ISO-14971 Risk Analysis WT : How to do a Process FMEA for Medical Devices after ISO-17791 Risk Analysis (PDF)
Process FMEA 004 What Is FMEA Failure Modes Effects Analysis 05-20-2015 WT : process FMEA (PDF)
Risk Analysis - Risk Analysis For Disposable Medical Devices 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
Risk Analysis 003 What Is ISO-14971 MDD-93-42-EEC Risk Analysis For Medical Devices CE Mark WT : Risk Analysis (PDF)
Pressure-sensitive Labels 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : pressure-sensitive labels (PDF)
When Quality Counts 009 What Are The Systems Validation Protocol Methods At ATL 05-28-2015 WT : When Quality Counts (PDF)
Process Capability - Process Capability For Disposable Medical Devices 008 How To Determine Process Capability For Medical Devices 05-19-2015 WT : Process Capability (PDF)

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