Tonometer AT 900 1420154

GUDID 07640132986051

Haag-Streit AG

Ophthalmic tonometer, manual

• Primary Device ID: 07640132986051
• NIH Device Record Key: e6800ae3-e090-483e-b8f5-4c881d56b91f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tonometer AT 900
• Version Model Number: Modell R
• Catalog Number: 1420154
• 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: false
• Serial Number: true
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640132986051 [Primary]

FDA Product Code

• HKY: Tonometer, Manual

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-16

On-Brand Devices [Tonometer AT 900]

• 07640132986907: Special color
• 07640132986068: Modell T
• 07640132986051: Modell R
• 07640132986044: Black
• 07640132986037: Grey
• 07640132986020: Modell BQ
• 07640132985962: Modell BQ