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Reliance Elara Tabletop

by Haag-Streit USA, Inc.

Reliance Elara Tabletop is a Class I device made by Haag-Streit USA, Inc., listed in FDA GUDID since 29 May 2026 (UDI-DI 00850020301638), 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 Number00850020301638 UDI-DI Date29 May 2026ListedStatusListed 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  • Withdrawn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
Static ophthalmic equipment stand, manually-adjusted
Model / reference
Elara Tabletop
Primary DI / UDI-DI
00850020301638
FDA product code
HMF
GMDN term
Static ophthalmic equipment stand, manually-adjusted
Device class
Class I
Regulation number
886.1860
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code HMF (Stand, Instrument, Ac-Powered, Ophthalmic).

Other devices from Haag-Streit USA, Inc.

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Properties

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