Taiwan FDA registration 0c99d9c15387a58ac8a4b7a5e61535df

"MITSUBISHI" MGC AnaeroPack incubation device (Non-Sterile)

TW: "三菱"細菌培養產氣包器材(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·MITSUBISHI GAS CHEMICAL COMPANY, INC.·Registered Oct 27, 2014 – Oct 27, 2024Expired
Registration details
Analysis ID
0c99d9c15387a58ac8a4b7a5e61535df
License Form
Ministry of Health Medical Device Import No. 014606
Customs Code
DHA09401460609
Company information
Manufacturer Country
Japan
Authorized Representative
GLOWAY CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of medical equipment management measures "Gas Production Equipment (C.2580)".
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C2580 Gas Production Equipment
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 27, 2014
Expiry Date
Oct 27, 2024
About this record

Access comprehensive regulatory information for "MITSUBISHI" MGC AnaeroPack incubation device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c99d9c15387a58ac8a4b7a5e61535df and manufactured by MITSUBISHI GAS CHEMICAL COMPANY, INC.. The authorized representative in Taiwan is GLOWAY CO., LTD..

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 DatabasePowered by Pure Global AI89,000+ Devices