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Na 00712808

by US Endoscopy

Ref 00712808Model Bite Blocks

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

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995ENBLOKLFSTRPT6 Basic UDI-DI 00724995184193UDI-DIDate19 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995184193 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

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

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  • Withdrawn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
Endoscopic bite block, basic, single-use
Device Name
Bite Blocks
Model / Ref / Catalog
00712808, Bite Blocks
Primary DI / UDI-DI
00724995184193
Basic UDI-DI
0724995ENBLOKLFSTRPT6
FDA Product Code
MNK
EMDN Code
G030804 Gastrointestinal endoscopy and echoendoscopy, bite blocks
GMDN Term
Endoscopic bite block, basic, single-use
Device Class
Class I
Regulation Number
876.1500
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Other devices from US Endoscopy

See all devices from US Endoscopy →

Properties

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

Other properties (18)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No