Taiwan FDA registration a39f8b27849f4e3080c14849ce17f559

"Yangpu" single-use vacuum blood collection tube (separation glue-procoagulant tube)

TW: “陽普”一次性使用真空採血管(分離膠-促凝管)

Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Sep 19, 2014 – Sep 19, 2029Active

Registration details

Analysis ID: a39f8b27849f4e3080c14849ce17f559
Customs Code: DHA09200062408

Company information

Manufacturer: GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: China
Authorized Representative: BEAM INTERNATIONAL INC.

Product details

Intended Use: It is used to collect blood for serochemical testing in clinical laboratories.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1675 Blood collection equipment
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Sep 19, 2014
Expiry Date: Sep 19, 2029

About this record

Access comprehensive regulatory information for "Yangpu" single-use vacuum blood collection tube (separation glue-procoagulant tube) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a39f8b27849f4e3080c14849ce17f559 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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