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Precisor 00388B

by Conmed Corporation

Listed FDA GUDID listing, not in commercial distribution

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10653405063841 UDI-DI Date24 Sep 2020ListedStatusListed GUDID: not 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  • Withdrawn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
Precisor
Generic Name
Flexible endoscopic biopsy forceps, single-use
Model / Ref / Catalog
00388B
Primary DI / UDI-DI
10653405063841
FDA Product Code
FCL
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class I
Regulation Number
876.1075
GUDID distribution status
Not in Commercial Distribution
Size
Length — 230 Centimeter
Outer Diameter — 2.3 Millimeter

Other devices from Conmed Corporation

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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