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Vapotherm

FDA UDI

by Vapotherm Inc.

Identity

Trade Name
Vapotherm FDA UDI
Generic Name
Freestanding/bed-attached intravenous pole FDA UDI
Device Name
Precision Flow Vapotherm Transfer Unit, DISS, India Version FDA UDI
Model / Reference
PF-VTU-DISS-OUS-IN FDA UDI
Description
Precision Flow Vapotherm Transfer Unit, DISS, India Version FDA UDI

Identifiers

Primary DI / UDI-DI
00841737104575 FDA UDI
GMDN Term
Freestanding/bed-attached intravenous pole FDA UDI

Classification

Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Freestanding/bed-attached intravenous poleSecondary battery

Vapotherm by Vapotherm Inc. — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Secondary battery.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vapotherm Inc.

Sources (1)

  • FDA UDI cdc80efd-414c-4e30-b3b8-09a37a5e4477 33 fields · synced May 30, 2026