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Vadi

FDA UDI

Class I (US FDA UDI)

by Vadi Medical Technology Co., Ltd.

Identity

Trade Name
VADI FDA UDI
Generic Name
Respiratory gas heating wire, adult FDA UDI
Device Name
Respiratory humidifier---Accessories- Heated wire (with port) FDA UDI
Model / Reference
900150L FDA UDI
Description
Respiratory humidifier---Accessories- Heated wire (with port) FDA UDI

Identifiers

Catalog Number
900150L-CFS FDA UDI
Primary DI / UDI-DI
04719894380902 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Respiratory gas heating wire, adult FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5975 FDA UDI
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

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Respiratory gas heating wire, adult

Vadi by Vadi Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Respiratory gas heating wire, adult.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vadi Medical Technology Co., Ltd.

Sources (1)

  • FDA UDI 91b36726-72b0-4612-a3b6-d311f7a6c2de 35 fields · synced Jun 1, 2026