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Single-Use Biopsy Forceps NBF03-01130230

by Micro-Tech (Nanjing) Co., Ltd. 2 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06932503540070 UDI-DI Date31 Dec 2021ListedStatusListed 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  • Withdrawn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
Single-Use Biopsy Forceps
Generic Name
Flexible endoscopic biopsy forceps, single-use
Model / Reference
NBF03-01130230
Description
New handle, Oval, with spike, Single outer sheath, PE coated, Four-bar linkage, 3.0*2300 mm
Primary DI / UDI-DI
06932503540070
FDA Product Code
FCL
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class I
Regulation Number
876.1075
GUDID distribution status
In Commercial Distribution
Size
Lumen/Inner Diameter — 3.2 Millimeter
Length — 230 Centimeter

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Other devices from Micro-Tech (Nanjing) Co., Ltd.

See all devices from Micro-Tech (Nanjing) Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (7)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No