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Precisor Broncho

by Conmed Corporation 3 variants

Ref 100502

Precisor Broncho (100502) is a device classified as Class IIa in the EU and Class I in the US made by Conmed Corporation, registered in EUDAMED on 2 Apr 2026 (Basic UDI-DI B-30653405052108) and listed in FDA GUDID since 28 Nov 2020 (UDI-DI 30653405052108), active as of 23 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDD

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-30653405052108 Basic UDI-DI 30653405052108UDI-DIDate2 Apr 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number30653405052108 UDI-DI Date28 Nov 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-30653405052108 registered 2 Apr 2026 Active
  • FDA GUDID UDI-DI 30653405052108 listed 28 Nov 2020 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 30653405052108
  2. Registered EUDAMED B-30653405052108

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic name
Flexible endoscopic biopsy forceps, single-use
Device name
Non-orthopedic, Non-active, Instrument, Endoscopic, Biopsy Forceps
Model / Ref / Catalog
100502
Primary DI / UDI-DI
30653405052108
Basic UDI-DI
B-30653405052108
FDA product code
FCL
EMDN code
G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
GMDN term
Flexible endoscopic biopsy forceps, single-use
Device class
Class IIa EUDAMED
Class I GUDID
Regulation number
876.1075
EU registration type
Legacy device (under a directive)
EU market of registration
Belgium
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Width — 1.8 Millimeter
Length — 115 Centimeter
Outer Diameter — 2 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Device classEUDAMED
Class IIa
GUDID
Class I
Sterilise before useEUDAMED
No
GUDID
Yes

Registry differences

EUDAMED and FDA GUDID describe the same product (same UDI-DI) and state different values:

  • Sterilise before use UDI-DI 30653405052108: EUDAMED states No, FDA GUDID states Yes.

Device class is stated on each registry's own scale: Class IIa in the EU (EUDAMED), Class I in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Similar devices in this category

Other devices filed under GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE.

Other devices from Conmed Corporation

See all devices from Conmed Corporation →

Properties

  • Supplied sterile
  • Sterilise before use NoEUDAMEDYesGUDID
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (18, all answered No)