Taiwan FDA registration 51cb7f62bdf32b542c48186534062c29
"VIMAP Technologies" Administration Set For Insufflators
TW: "邁美科技" 腹腔消化道套組
Taiwan·Risk Class 2·MD·INNOVATIVE MEDICAL MANUFACTURING COMPANY·Registered Sep 15, 2015 – Sep 15, 2025ExpiredRegistration details
- Analysis ID
- 51cb7f62bdf32b542c48186534062c29
- License Form
- Ministry of Health Medical Device Manufacturing No. 005068
Company information
- Manufacturer
- INNOVATIVE MEDICAL MANUFACTURING COMPANY
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- INNOVATIVE MEDICAL MANUFACTURING COMPANY
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 15, 2015
- Expiry Date
- Sep 15, 2025
About this record
Access comprehensive regulatory information for "VIMAP Technologies" Administration Set For Insufflators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 51cb7f62bdf32b542c48186534062c29 and manufactured by INNOVATIVE MEDICAL MANUFACTURING COMPANY. The authorized representative in Taiwan is INNOVATIVE MEDICAL MANUFACTURING COMPANY.
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