Taiwan FDA registration 86fe8ee568c19af9df3a26f12277abf4

Single-use vacuum blood collection tubes (ESI)

TW: 陽普一次性使用真空採血管(血沉管)

Taiwan·Risk Class 2·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Dec 11, 2014 – Dec 11, 2029Active

Registration details

Analysis ID: 86fe8ee568c19af9df3a26f12277abf4
Customs Code: DHA09200063003

Company information

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

Product details

Intended Use: This product is mainly used for the detection of blood cell sedimentation rate, and the reference method is Wechsler erythrocyte sedimentation rate.
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: Dec 11, 2014
Expiry Date: Dec 11, 2029

About this record

Access comprehensive regulatory information for Single-use vacuum blood collection tubes (ESI) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 86fe8ee568c19af9df3a26f12277abf4 and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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