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BL Clamp CLAPM12A

by B& L Biotech, inc.

BL Clamp CLAPM12A is a Class I device made by B& L Biotech, inc., listed in FDA GUDID since 18 Jul 2025 (UDI-DI 08800019151029), 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 Number08800019151029 UDI-DI Date18 Jul 2025ListedStatusListed 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  • Withdrawn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
BL Clamp
Generic name
Rubber dam clamp
Model / reference
CLAPM12A
Primary DI / UDI-DI
08800019151029
FDA product code
EJG
GMDN term
Rubber dam clamp
Device class
Class I
Regulation number
872.6300
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rubber dam clamp

Similar devices

Other devices filed under FDA product code EJG (Forceps, Rubber Dam Clamp).

Other devices from B&L Biotech Co., Ltd.

See all devices from B&L Biotech Co., Ltd. →

Properties

  • Sterilise before use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)