Remel R02050

Remel R02050 is a Class I device made by Remel, Inc., listed in FDA GUDID since 29 Dec 2022 (UDI-DI 00848838003707), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00848838003707 UDI-DI	Date29 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00848838003707

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name: Remel
Generic name: Differential/selective agar culture medium IVD
Model / Ref / Catalog: R02050

Primary DI / UDI-DI: 00848838003707
FDA product code: JSI
GMDN term: Differential/selective agar culture medium IVD

Device class: Class I
Regulation number: 866.2360
GUDID distribution status: In Commercial Distribution

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Properties

Premarket exempt
Lot / batch number
Expiration date

Other properties (12, all answered No)