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Locktite 11090

by B&B Medical Technologies, Inc

Ref 11090

Locktite 11090 is a Class I device made by B&B Medical Technologies, Inc, registered in EUDAMED on 17 Sep 2026 (Basic UDI-DI 08500087331109072) and listed in FDA GUDID since 29 Jan 2020 (UDI-DI 00850008733130), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number08500087331109072 Basic UDI-DI 00850008733130UDI-DIDate17 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00850008733130 UDI-DI Date29 Jan 2020ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 08500087331109072 registered 17 Sep 2026 Active
  • FDA GUDID UDI-DI 00850008733130 listed 29 Jan 2020 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 00850008733130
  2. Registered EUDAMED 08500087331109072

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  • Withdrawn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

Trade name
Locktite
Generic name
Endotracheal tube holder
Model / Ref / Catalog
11090
Primary DI / UDI-DI
00850008733130
Basic UDI-DI
08500087331109072
FDA product code
CBH
EMDN code
R018002 Intubation device supports
GMDN term
Endotracheal tube holder
Device class
Class I
Regulation number
868.5770
EU registration type
Standard device
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endotracheal tube holder

Similar devices in this category

Other devices filed under INTUBATION DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES.

Other devices from B&B Medical Technologies, Inc

See all devices from B&B Medical Technologies, Inc →

Properties

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