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Aesculap BF310ZR

by Aesculap, Inc.

Aesculap BF310ZR is a Class I device made by Aesculap, Inc., listed in FDA GUDID since 1 Aug 2022 (UDI-DI 04046955652518), 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 Number04046955652518 UDI-DI Date1 Aug 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  • Withdrawn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
Aesculap
Generic name
Towel clamp, reusable
Model / Ref / Catalog
BF310ZR
Primary DI / UDI-DI
04046955652518
FDA product code
HTD
GMDN term
Towel clamp, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Towel clamp, reusable

Similar devices in this category

Other devices filed under Towel clamp, reusable.

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)