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00712803

by US Endoscopy

Ref 00712803Model Bite Blocks

00712803 is a Class I device made by US Endoscopy, registered in EUDAMED on 19 Aug 2026 (Basic UDI-DI 0724995ENBBLOCKSTRAPL2) and listed in FDA GUDID since 31 Mar 2021 (UDI-DI 00724995184155), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995ENBBLOCKSTRAPL2 Basic UDI-DI 00724995184155UDI-DIDate19 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995184155 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0724995ENBBLOCKSTRAPL2 registered 19 Aug 2026 Active
  • FDA GUDID UDI-DI 00724995184155 listed 31 Mar 2021 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 00724995184155
  2. Registered EUDAMED 0724995ENBBLOCKSTRAPL2

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  • Withdrawn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
00712803, Bite Blocks
Primary DI / UDI-DI
00724995184155
Basic UDI-DI
0724995ENBBLOCKSTRAPL2
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 registration type
Standard device
EU market of registration
Ireland
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under GASTROINTESTINAL ENDOSCOPY AND ECHOENDOSCOPY, BITE BLOCKS.

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 (19, all answered No)