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Puritan Bennett 10084332

by Covidien LP

Puritan Bennett 10084332 is a Class II device made by Covidien LP, listed in FDA GUDID since 22 Feb 2018 (UDI-DI 30884521252954), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number30884521252954 UDI-DI Date22 Feb 2018ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Puritan Bennett
Generic name
Ventilator application software
Model / reference
10084332
Primary DI / UDI-DI
30884521252954
FDA product code
CBK
GMDN term
Ventilator application software
Device class
Class II
Regulation number
868.5895
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CBK (VENTILATOR, CONTINUOUS, FACILITY USE).

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

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)