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Precisor 00820C

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 Number30653405052061 UDI-DI Date4 Jun 2018ListedStatusListed 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  • Withdrawn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
00820C
Primary DI / UDI-DI
30653405052061
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
Outer Diameter — 3.1 Millimeter
Length — 230 Centimeter

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

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