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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
Ventilator breathing circuit, reusable FDA UDI
Device Name
Reusable ventilator circuit/ tubing (Without heated wire) FDA UDI
Model / Reference
G-328001-1 FDA UDI
Description
Reusable ventilator circuit/ tubing (Without heated wire) FDA UDI

Identifiers

Catalog Number
G-328001-1-CFS FDA UDI
Primary DI / UDI-DI
04719894380896 FDA UDI
FDA Product Code
BZO FDA UDI
GMDN Term
Ventilator breathing circuit, reusable 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: Ventilator breathing circuit, reusable

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

Similar devices

Also classified as Ventilator breathing circuit, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI aa34fa76-eefc-4e97-a90d-3eab0c999027 35 fields · synced May 29, 2026