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Remel R060146

by Remel, Inc.

Remel R060146 is a Class I device made by Remel, Inc., listed in FDA GUDID since 23 Dec 2022 (UDI-DI 00848838005763), 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 Number00848838005763 UDI-DI Date23 Dec 2022ListedStatusListed 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  • Withdrawn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
Remel
Generic name
Culture medium control
Model / Ref / Catalog
R060146
Primary DI / UDI-DI
00848838005763
FDA product code
JSF
GMDN term
Culture medium control
Device class
Class I
Regulation number
866.2320
GUDID distribution status
In Commercial Distribution

Related devices

Category: Culture medium control

Similar devices

Also classified as Culture medium control.

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)