Taiwan FDA registration 37e6d4875bd2c23669b0846cfa0e0a6c

"Gynemed" Enriched culture medium (Non-sterile)

TW: "吉耐美"強化培養基 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·GYNEMED MEDIZINPRODUKTE GMBH & CO. KG·Registered Aug 12, 2015 – Aug 12, 2020Cancelled
Registration details
Analysis ID
37e6d4875bd2c23669b0846cfa0e0a6c
License Form
Ministry of Health Medical Device Import No. 015572
Customs Code
DHA09401557200
Company information
Manufacturer Country
Germany
Authorized Representative
PSUCHE TECHNOLOGY CO., LTD.
Product details
Product Type (Level 1)
C Immunology and microbiology devices
Product Type (Level 2)
C2330 Bacterial culture media
Import Information
Imported from abroad
Dates and status
Registration Date
Aug 12, 2015
Expiry Date
Aug 12, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Gynemed" Enriched culture medium (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 37e6d4875bd2c23669b0846cfa0e0a6c and manufactured by GYNEMED MEDIZINPRODUKTE GMBH & CO. KG. The authorized representative in Taiwan is PSUCHE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GYNEMED MEDIZINPRODUKTE GMBH & CO. KG, and 1 recent registrations in the same category. 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.

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