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710201

by US Endoscopy

Ref 710201Model Polyp Traps - Non-Sterile

710201 is a device classified as Class I in the EU and Class II in the US made by US Endoscopy, registered in EUDAMED on 2 Nov 2026 (Basic UDI-DI 0724995ENQUIKCATCHNS7R) and listed in FDA GUDID since 24 Jun 2022 (UDI-DI 00724995184704), active as of 7 Nov 2026.

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

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, GUDID, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995ENQUIKCATCHNS7R Basic UDI-DI 00724995184704UDI-DIDate2 Nov 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995184704 UDI-DI Date24 Jun 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995ENQUIKCATCHNS7R registered 2 Nov 2026 Active
  • FDA GUDID UDI-DI 00724995184704 listed 24 Jun 2022 Listed

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Timeline

2 dated events

  1. Listed FDA GUDID 00724995184704
  2. Registered EUDAMED 0724995ENQUIKCATCHNS7R

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Generic name
General specimen receptacle transport container
Device name
Polyp Traps - Non-Sterile
Model / Ref / Catalog
710201, Polyp Traps - Non-Sterile
Primary DI / UDI-DI
00724995184704
Basic UDI-DI
0724995ENQUIKCATCHNS7R
FDA product code
KDQ
EMDN code
G03050199 Digestive endoscopy, retrieval devices - other
GMDN term
General specimen receptacle transport container
Device class
Class I EUDAMED
Class II GUDID
Regulation number
880.6740
EU registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

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

Related devices

Category: General specimen receptacle transport container

Similar devices in this category

Other devices filed under DIGESTIVE ENDOSCOPY, RETRIEVAL DEVICES - OTHER.

Other devices from US Endoscopy

See all devices from US Endoscopy →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (20, all answered No)