Taiwan FDA registration f81c995fc3a10eb6f2d88fa6c9649c3f

"West Sea" Microbial Sample Collection and Delivery Equipment (Unsterilized)

TW: "西海" 微生物樣本收集及輸送器材 (未滅菌)

Taiwan·Risk Class 1·DNA GENOTEK INC.·Registered Apr 19, 2013 – Apr 19, 2018Cancelled

Registration details

Analysis ID: f81c995fc3a10eb6f2d88fa6c9649c3f
Customs Code: DHA04401292601

Company information

Manufacturer: DNA GENOTEK INC.
Manufacturer Country: Canada
Authorized Representative: SEEHIGH BIOTECH CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2900 Microbial sample collection and delivery equipment
Import Information: import

Dates and status

Registration Date: Apr 19, 2013
Expiry Date: Apr 19, 2018
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "West Sea" Microbial Sample Collection and Delivery Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f81c995fc3a10eb6f2d88fa6c9649c3f and manufactured by DNA GENOTEK INC.. The authorized representative in Taiwan is SEEHIGH BIOTECH CO., LTD..

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