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Aesculap BN750R

by Aesculap AG

Aesculap BN750R is a Class I device made by Aesculap AG, listed in FDA GUDID since 17 Apr 2020 (UDI-DI 04038653029662), registry data as of 12 Nov 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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04038653029662 UDI-DI Date17 Apr 2020ListedStatusListed 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  • Withdrawn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
Skin staple remover, reusable
Model / Ref / Catalog
BN750R
Primary DI / UDI-DI
04038653029662
FDA product code
HTD
GMDN term
Skin staple remover, 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: Skin staple remover, reusable

Similar devices

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

Other devices from Aesculap AG

See all devices from Aesculap AG →

Properties

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