Taiwan FDA registration 927ed05de0b155a6b82e17ceb2862d25

"Inmeve" Bacterial Pneumonia 2-in-1 Test Kit (Unsterilized)

TW: "茵美芙" 細菌性肺炎二合一檢測組劑 (未滅菌)

Taiwan·Risk Class 1·STATENS SERUM INSTITUT·Registered Mar 22, 2016 – Mar 22, 2021Cancelled

Registration details

Analysis ID: 927ed05de0b155a6b82e17ceb2862d25
Customs Code: DHA09401629706

Company information

Manufacturer: STATENS SERUM INSTITUT
Manufacturer Country: Denmark
Authorized Representative: GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the management method of medical equipment, Haemophilus serological reagent (C.3300) and streptococcus serum reagent (C.3740) The first level identification range is limited.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3300 嗜血桿菌屬血清試劑;; C.3740 鏈球菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Mar 22, 2016
Expiry Date: Mar 22, 2021
Cancellation Date: Aug 15, 2023

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Inmeve" Bacterial Pneumonia 2-in-1 Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 927ed05de0b155a6b82e17ceb2862d25 and manufactured by STATENS SERUM INSTITUT. The authorized representative in Taiwan is GHOPE INTERNATIONAL BIOTECHNOLOGY CO., LTD..

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