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Forceps Pean Forceps

by Dr.frigz International(Pvt)Ltd, 7 variants

Forceps Pean Forceps (12200) is a Class I device made by Dr.frigz International(Pvt)Ltd,, listed in FDA GUDID since 22 Nov 2022 (UDI-DI B974122000), 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 NumberB974122000 UDI-DI Date22 Nov 2022ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Forceps
Generic name
Dressing/utility forceps, scissors-like, single-use
Model / Ref / Catalog
PEAN FORCEPS, 12200
Primary DI / UDI-DI
B974122000
FDA product code
GEN
GMDN term
Dressing/utility forceps, scissors-like, single-use
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Length — 18.5 Centimeter

Related devices

Category: Dressing/utility forceps, scissors-like, single-use

Similar devices in this category

Other devices filed under Dressing/utility forceps, scissors-like, single-use.

Other devices from Dr.frigz International(Pvt)Ltd,

See all devices from Dr.frigz International(Pvt)Ltd, →

Properties

  • Sterilise before use
  • Single use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)