Pure Global

"Bioken" mumps virus test reagent (unsterilized) - Taiwan Registration a4427d2da2004237f66179e1b8279d68

Access comprehensive regulatory information for "Bioken" mumps virus test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a4427d2da2004237f66179e1b8279d68 and manufactured by DENKA CO., LTD. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
a4427d2da2004237f66179e1b8279d68
Registration Details
Taiwan FDA Registration: a4427d2da2004237f66179e1b8279d68
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Bioken" mumps virus test reagent (unsterilized)
TW: "็”Ÿ็ ”" ่…ฎ่…บ็‚Ž็—…ๆฏ’ๆชข้ฉ—่ฉฆๅŠ‘ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

a4427d2da2004237f66179e1b8279d68

DHA04401282900

Company Information

Japan

Product Details

It is limited to the first-level identification scope of the "Mumps Virus Serum Reagent (C.3380)" of the Measures for the Classification and Grading of Medical Devices.

C Immunology and microbiology

C.3380 ่…ฎ่…บ็‚Ž็—…ๆฏ’่ก€ๆธ…่ฉฆๅŠ‘

import

Dates and Status

Mar 22, 2013

Mar 22, 2028