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Fisherbrand 238017P

by Fisher Scientific Company L.L.C.

Fisherbrand 238017P (08953B) is a Class I device made by Fisher Scientific Company L.L.C., listed in FDA GUDID since 19 Sep 2022 (UDI-DI 00613647010105), 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 Number00613647010105 UDI-DI Date19 Sep 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  • Withdrawn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
Fisherbrand
Generic name
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Model / Ref / Catalog
238017P, 08953B
Primary DI / UDI-DI
00613647010105
FDA product code
GEN
GMDN term
Surgical soft-tissue manipulation forceps, tweezers-like, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Similar devices in this category

Other devices filed under Surgical soft-tissue manipulation forceps, tweezers-like, reusable.

Other devices from Fisher Scientific Company L.L.C.

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Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)