Taiwan FDA registration 26eec191a0bfc9eeea9032b69d60bb14
"Miacom" respiFISH Masterpanel (Non-sterile)
TW: "麥康" 螢光呼吸原位雜交探針 (未滅菌)
Taiwan·Risk Class 1·MD·MIACOM DIAGNOSTICS GMBH·Registered Dec 21, 2015 – Dec 21, 2020CancelledRegistration details
- Analysis ID
- 26eec191a0bfc9eeea9032b69d60bb14
- License Form
- Ministry of Health Medical Device Import No. 016004
- Customs Code
- DHA09401600404
Company information
- Manufacturer
- MIACOM DIAGNOSTICS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ARSENALS IVD CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 21, 2015
- Expiry Date
- Dec 21, 2020
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Miacom" respiFISH Masterpanel (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 26eec191a0bfc9eeea9032b69d60bb14 and manufactured by MIACOM DIAGNOSTICS GMBH. The authorized representative in Taiwan is ARSENALS IVD CO., LTD..
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