Contact glass 903 1400291

GUDID 07640132986310

Haag-Streit AG

Diagnostic condensing lens

• Primary Device ID: 07640132986310
• NIH Device Record Key: b54e4a3a-37d1-401d-9442-9e9c5f239ef9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Contact glass 903
• Version Model Number: 903
• Catalog Number: 1400291
• Company DUNS: 483467544
• Company Name: Haag-Streit AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +41319780111
• Email: service@haag-streit.com
• Phone: +41319780111
• Email: service@haag-streit.com
• Phone: +41319780111
• Email: service@haag-streit.com
• Phone: +41319780111
• Email: service@haag-streit.com
• Phone: +41319780111
• Email: service@haag-streit.com
• Phone: +41319780111
• Email: service@haag-streit.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640132986310 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K051103

FDA Product Code

• HJK: Lens, Contact, Polymethylmethacrylate, Diagnostic

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-23

On-Brand Devices [Contact glass 903]

• 07640132986334: 903 without ring
• 07640132986310: 903