Taiwan FDA registration 4443d17476848f2cfd3430651431b785

"AirLife" Arterial blood sampling kit (NON-STERILE)

TW: "愛樂活" 動脈血液取樣組 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.·Registered Feb 23, 2017 – Feb 23, 2022Cancelled
Registration details
Analysis ID
4443d17476848f2cfd3430651431b785
License Form
Ministry of Health Medical Device Import No. 017518
Customs Code
DHA09401751801
Company information
Manufacturer Country
Mexico
Authorized Representative
PHOENIX INSTRUMENT BUSINESS CO., LTD.
Product details
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D1100 Arterial blood sampling group
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 23, 2017
Expiry Date
Feb 23, 2022
Cancellation Date
Mar 30, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "AirLife" Arterial blood sampling kit (NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4443d17476848f2cfd3430651431b785 and manufactured by PRODUCTOS UROLOGOS DE MEXICO S.A. DE C.V.. The authorized representative in Taiwan is PHOENIX INSTRUMENT BUSINESS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices