Taiwan FDA registration 6372f3212d325627e090fbefdd0102ca

"Taifu" Solodine ATG test reagent

TW: "台富" 速樂定ATG檢驗試劑

Taiwan·Risk Class 2·Taiwan Fu Pharmaceutical Co., Ltd·Registered Dec 02, 2005 – Dec 02, 2015Cancelled

Registration details

Analysis ID: 6372f3212d325627e090fbefdd0102ca

Company information

Manufacturer: Taiwan Fu Pharmaceutical Co., Ltd
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Taiwan Fu Pharmaceutical Co., Ltd

Product details

Intended Use: 被動粒子凝集法測定受檢者血清中之anti-thyroglobulin抗體.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.5870 甲狀腺自體抗體免疫試驗系統
Import Information: import

Dates and status

Registration Date: Dec 02, 2005
Expiry Date: Dec 02, 2015
Cancellation Date: May 17, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Taifu" Solodine ATG test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6372f3212d325627e090fbefdd0102ca and manufactured by Taiwan Fu Pharmaceutical Co., Ltd. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.

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