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Vapotherm HVT-UKIT-JP

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 Number00841737105893 UDI-DI Date19 Nov 2025ListedStatusListed 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  • Withdrawn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
Professional high-flow respiratory unit, humidifying, manual
Model / reference
HVT-UKIT-JP
Primary DI / UDI-DI
00841737105893
FDA product code
BTT
GMDN term
Professional high-flow respiratory unit, humidifying, manual
Device class
Class II
Regulation number
868.5450
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Other devices from Vapotherm Inc.

See all devices from Vapotherm Inc. →

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date

Other properties (11)

  • Supplied sterile: No
  • Sterilise before use: No
  • Implantable: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Manufacturing date: No