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Aesculap MB232

by Aesculap, Inc.

Aesculap MB232 is a Class I device made by Aesculap, Inc., listed in FDA GUDID since 5 Jun 2026 (UDI-DI 04046964683039), 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 Number04046964683039 UDI-DI Date5 Jun 2026ListedStatusListed 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  • Withdrawn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
Aesculap
Generic name
Surgical bulldog clamp, reusable
Model / Ref / Catalog
MB232
Primary DI / UDI-DI
04046964683039
FDA product code
HTD
GMDN term
Surgical bulldog clamp, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code HTD (FORCEPS).

Other devices from Aesculap, Inc.

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Properties

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