Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9616445

FEI Number

3005749238

Entity Name

VADI Medical Technology Co., Ltd.

City/State/Country

Taoyuan City, TW

Establishment Address

No.198, Lane 298, Huandong Road, Zhongshan Village, Yangmei District, Taoyuan City 32665, TW

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

VADI Medical Technology Co., Ltd. (Owner Number: 9040244)

Owner / Operator Contact Address

No.198, Lane 298, Huandong Road, Zhongshan Village, Yangmei District, Taoyuan City, TW-TAO 32665, TW

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

VADI VARIOUS MODELS VADI Oxygen Pressure Tube VADI VARIOUS MODELS OF HEATER VADI OXYGEN MIXING BAG VADI WATER TRAP Airway Connector VADI NASAL CANNULA ANESTHETIC GAS

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
CAI	Circuit, Breathing (W Connector, Adaptor, Y Piece)	Anesthesiology	Class 1	868.5240	2007-04-06
BYX	Tubing, Pressure And Accessories	Anesthesiology	Class 1	868.5860	2025-04-08
IRQ	Unit, Heating, Powered	Physical Medicine	Class 1	890.5950	2007-03-30
BTC	Bag, Reservoir	Anesthesiology	Class 1	868.5320	2000-10-06
BYH	Drain, Tee (Water Trap)	Anesthesiology	Class 1	868.5995	2003-06-17
BZA	Connector, Airway (Extension)	Anesthesiology	Class 1	868.5810	2024-09-24
CAT	Cannula, Nasal, Oxygen	Anesthesiology	Class 1	868.5340	2000-10-06
BSJ	Mask, Gas, Anesthetic	Anesthesiology	Class 1	868.5550	2000-01-27

Official Correspondent

Wei-Shin HUANG

US Agent Details

Fanny Zhao Business: J & F Technology Service Email: info@jf-yiliao.com Phone: (909) 5100201

Related Public Records

Same Entity

VADI Medical Technology Co., Ltd.

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0033-04	VIASYS Med Systems	1	Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube with Bird adapter, oxygen supply tubing, sideport connector with adjustable bleed valve, and 40 cm H2O Popoff elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83124-2
Z-0034-04	VIASYS Med Systems	1	Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, ported elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83100-24
Z-0035-04	VIASYS Med Systems	1	Neonatal/Infant Hyperinflation Circuit, consisting of a 0.5 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve, 40 cm H2O Popoff elbow and infant mask; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83144-24
Z-0036-04	VIASYS Med Systems	1	Hyperinflation Circuit, consisting of a 2.0 L breathing bag, pressure monitoring tube, oxygen supply tubing, sideport connector with adjustable bleed valve and ported elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83120
Z-0037-04	VIASYS Med Systems	1	Sideport Kit, consisting of an adjustable sideport valve and an O2 port elbow; Mfg. for Corpak MedSystems, Wheeling, IL 60090; 20 units per case; reorder #BLD-83166

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9616445. Last updated year: 2026. Please use registration number 9616445 when referencing this establishment in official correspondence.