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Single-Use Biopsy Forceps BF-F-1.8×600

by MacroLux Medical Technology 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 2 Nov 2026. What this means

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06975339628871 UDI-DI Date19 Oct 2026ListedStatusListed 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  • Withdrawn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
BF-F-1.8×600
Primary DI / UDI-DI
06975339628871
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
MRI Safety
MR Unsafe

Other devices from MacroLux Medical Technology Co., Ltd.

See all devices from MacroLux Medical Technology Co., Ltd. →

Properties

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

Other properties (8)

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