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Cenmed 2110005

by Biochemical Diagnostics Inc

Cenmed 2110005 (18000347) is a Class I device made by Biochemical Diagnostics Inc, listed in FDA GUDID since 29 Jun 2021 (UDI-DI 00810042683129), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810042683129 UDI-DI Date29 Jun 2021ListedStatusListed 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  • Withdrawn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
Cenmed
Generic name
Human chorionic gonadotropin beta-core fragment IVD, control
Model / Ref / Catalog
2110005, 18000347
Primary DI / UDI-DI
00810042683129
FDA product code
JJX
GMDN term
Human chorionic gonadotropin beta-core fragment IVD, control
Device class
Class I
Regulation number
862.1660
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JJX (Single (Specified) Analyte Controls (Assayed And Unassayed)).

Other devices from Biochemical Diagnostics Inc

See all devices from Biochemical Diagnostics Inc →

Properties

  • Lot / batch number
  • Expiration date
Other properties (13, all answered No)