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Vapotherm HiVNI-UKIT-DK

by Vapotherm Inc.

Vapotherm HiVNI-UKIT-DK is a Class II device made by Vapotherm Inc., listed in FDA GUDID since 22 Feb 2019 (UDI-DI 00841737102649), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00841737102649 UDI-DI Date22 Feb 2019ListedStatusListed 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  • Withdrawn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
Electrical mains power cable
Model / reference
HiVNI-UKIT-DK
Primary DI / UDI-DI
00841737102649
FDA product code
QAV
GMDN term
Electrical mains power cable
Device class
Class II
Regulation number
868.5454
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

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Properties

  • Convenience kit
Other properties (14, all answered No)