Taiwan FDA registration 9889ba7a0e9be645ef1a735102ef85f2

"Hede" platelet storage container (unsterilized)

TW: "和德" 血小板貯存容器 (未滅菌)

Taiwan·Risk Class 1·HOTECH INSTRUMENTS CORP.·Registered Nov 18, 2008 – Nov 18, 2028Active

Registration details

Analysis ID: 9889ba7a0e9be645ef1a735102ef85f2

Company information

Manufacturer: HOTECH INSTRUMENTS CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HOTECH INSTRUMENTS CORP.

Product details

Intended Use: It is limited to the first-level identification scope of the "Environmental Control Box for Preserving Platelet Concentrate (B.9575)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): B Hematology, pathology, and genetics
Product Type (Level 2): B.9575 Environmental control chamber for storing platelet concentrate
Import Information: Domestic

Dates and status

Registration Date: Nov 18, 2008
Expiry Date: Nov 18, 2028

About this record

Access comprehensive regulatory information for "Hede" platelet storage container (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9889ba7a0e9be645ef1a735102ef85f2 and manufactured by HOTECH INSTRUMENTS CORP.. The authorized representative in Taiwan is HOTECH INSTRUMENTS CORP..

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