Tonometer AT 870 1001310

GUDID 07640132986082

Haag-Streit AG

Ophthalmic tonometer, manual

• Primary Device ID: 07640132986082
• NIH Device Record Key: 4dbf735a-5338-4b97-9f8f-69875d0eca3a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Tonometer AT 870
• Version Model Number: n/a
• Catalog Number: 1001310
• 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	07640132986082 [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 870]

• 07640132986082: n/a
• 07640132985979: n/a