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Reliance Chair Glide

by Haag-Streit USA, Inc. 2 variants

Reliance Chair Glide (729600) is a Class I device made by Haag-Streit USA, Inc., listed in FDA GUDID since 9 Sep 2020 (UDI-DI 00850020301102), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850020301102 UDI-DI Date9 Sep 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Reliance
Generic name
Ophthalmic chair, manual
Model / Ref / Catalog
Chair Glide, 729600
Primary DI / UDI-DI
00850020301102
FDA product code
HME
GMDN term
Ophthalmic chair, manual
Device class
Class I
Regulation number
886.1140
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HME (Chair, Ophthalmic, Ac-Powered).

Other devices from Haag-Streit USA, Inc.

See all devices from Haag-Streit USA, Inc. →

Properties

  • Premarket exempt
Other properties (14, all answered No)