Taiwan FDA registration b66e9e4da4428bd3e108403d1e00ad72

Fuji Ammonia Analyzer (Unsterilized)

TW: 富士血氨分析儀 (未滅菌)

Taiwan·Risk Class 1·FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE·Registered Dec 15, 2009 – Dec 15, 2014Cancelled

Registration details

Analysis ID: b66e9e4da4428bd3e108403d1e00ad72
Customs Code: DHA04400838807

Company information

Manufacturer: FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE
Manufacturer Country: Japan
Authorized Representative: HUNG CHONG CORP.

Product details

Intended Use: Limited to the first level identification range of the blood ammonia test system (A.1065) of the management method for medical equipment.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1065 血氨試驗系統
Import Information: import

Dates and status

Registration Date: Dec 15, 2009
Expiry Date: Dec 15, 2014
Cancellation Date: Apr 25, 2018

Cancellation information

Status: Logged out
Reason: 自行鍵入

About this record

Access comprehensive regulatory information for Fuji Ammonia Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b66e9e4da4428bd3e108403d1e00ad72 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is HUNG CHONG CORP..

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