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Remel R09652

by Remel, Inc.

Remel R09652 is a Class I device made by Remel, Inc., listed in FDA GUDID since 4 Jan 2023 (UDI-DI 00848838013386), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00848838013386 UDI-DI Date4 Jan 2023ListedStatusListed GUDID: not 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  • Withdrawn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
Remel
Generic name
Culture medium base ingredient IVD
Model / Ref / Catalog
R09652
Primary DI / UDI-DI
00848838013386
FDA product code
LIB
GMDN term
Culture medium base ingredient IVD
Device class
Class I
Regulation number
866.2660
GUDID distribution status
Not in Commercial Distribution

Other devices from Remel, Inc.

See all devices from Remel, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (12, all answered No)