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Puritan Bennett 180-05

by Covidien LP

Ref 180-05

Puritan Bennett 180-05 is an artificial airway tube cuff pressure monitor (EU MDR Class I; FDA Class II; FDA product code BSK, Cuff, tracheal tube, inflatable) made by Covidien LP, registered in EUDAMED on 20 Aug 2026 (Basic UDI-DI 0763000B00006267W) and listed in FDA GUDID since 7 Jun 2021 (UDI-DI 10884521782501), active as of 23 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 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/MDR EUDAMED Number0763000B00006267W Basic UDI-DI 10884521782501UDI-DIDate20 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number10884521782501 UDI-DI Date7 Jun 2021ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 0763000B00006267W registered 20 Aug 2026 Active
  • FDA GUDID UDI-DI 10884521782501 listed 7 Jun 2021 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 10884521782501
  2. Registered EUDAMED 0763000B00006267W

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  • Withdrawn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
Puritan Bennett
Generic name
Artificial airway tube cuff pressure monitor
Device name
Puritan Bennett™ Extension Tube
Model / reference
180-05
Primary DI / UDI-DI
10884521782501
Basic UDI-DI
0763000B00006267W
FDA product code
BSK
EMDN code
R01038001 Endotracheal tube cuffs inflation systems
GMDN term
Artificial airway tube cuff pressure monitor
Device class
Class I EUDAMED
Class II GUDID
Regulation number
868.5750
EU registration type
Standard device
EU market of registration
Netherlands
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: Artificial airway tube cuff pressure monitor

Similar devices in this category

Other devices filed under ENDOTRACHEAL TUBE CUFFS INFLATION SYSTEMS.

Other devices from Covidien LP

  • LigaSure MRASILF19

    Class II

  • Shiley 110860

    Class II

  • Shiley 110865

    Class II

  • Shiley 110870

    Class II

See all devices from Covidien LP →

Properties

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