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Reliance

FDA UDI

Class I (US FDA UDI)

by Haag-Streit Usa, Inc.

Identity

Trade Name
Reliance FDA UDI
Generic Name
Ophthalmic chair, manual FDA UDI
Model / Reference
Chair Glide FDA UDI

Identifiers

Catalog Number
729600 FDA UDI
Primary DI / UDI-DI
00850020301102 FDA UDI
FDA Product Code
HME FDA UDI
GMDN Term
Ophthalmic chair, manual FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1140 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Ophthalmic chair, manual

Reliance by Haag-Streit Usa, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic chair, manual.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d38c5f2d-42ee-40aa-bcb0-bc8b2d72423d 33 fields · synced Jun 1, 2026