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Vapotherm PF-Plus-UKIT-DK

by Vapotherm Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841737102175 UDI-DI Date28 Sep 2017ListedStatusListed 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  • Withdrawn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
Vapotherm
Generic name
Respiratory oxygen sensor
Model / reference
PF-Plus-UKIT-DK
Primary DI / UDI-DI
00841737102175
GMDN term
Respiratory oxygen sensor
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Respiratory oxygen sensorElectrical mains power cable

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Properties

  • Convenience kit

Other properties (14)

  • Supplied sterile: No
  • Sterilise before use: No
  • Single use: No
  • Implantable: No
  • Contains latex: No
  • Prescription use: No
  • Over-the-counter: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Lot / batch number: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No