Haag-Streit Surgical

GUDID 00850020301522

Practitioner positioning chair/ stool for treatment and examination

HAAG-STREIT USA, INC.

General-purpose stool/chair

• Primary Device ID: 00850020301522
• NIH Device Record Key: 57468e20-640e-4712-8905-ab0662ecaefd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Haag-Streit Surgical
• Version Model Number: 900 Surgical Chair
• Company DUNS: 080962286
• Company Name: HAAG-STREIT USA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850020301522 [Primary]

FDA Product Code

• HMD: Chair, Ophthalmic, Manual

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-11
• Device Publish Date: 2024-01-03

Devices Manufactured by HAAG-STREIT USA, INC.

• 00850020301522 - Haag-Streit Surgical: 2024-01-11Practitioner positioning chair/ stool for treatment and examination
• 00850020301522 - Haag-Streit Surgical: 2024-01-11 Practitioner positioning chair/ stool for treatment and examination
• 00850020301003 - Reliance: 2020-09-17
• 00850020301010 - Reliance: 2020-09-17
• 00850020301027 - Reliance: 2020-09-17
• 00850020301034 - Reliance: 2020-09-17
• 00850020301041 - Reliance: 2020-09-17
• 00850020301058 - Reliance: 2020-09-17
• 00850020301065 - Reliance: 2020-09-17