Taiwan FDA registration 2209ce19ecbcd8fecfb9e7d34fb4ee74
“FUJIFILM medwork” Polypectomy Snare POL-Series
TW: "富士 美德沃"瘜肉切除環
Taiwan·Risk Class 2·MD·FUJIFILM medwork GmbH·Registered Apr 11, 2023 – Apr 11, 2028ActiveRegistration details
- Analysis ID
- 2209ce19ecbcd8fecfb9e7d34fb4ee74
- License Form
- Ministry of Health Medical Device Import No. 036462
- Customs Code
- DHA05603646200
Company information
- Manufacturer
- FUJIFILM medwork GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- FUJIFILM HEALTHCARE TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H4300 Electrosurgical device for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 11, 2023
- Expiry Date
- Apr 11, 2028
About this record
Access comprehensive regulatory information for “FUJIFILM medwork” Polypectomy Snare POL-Series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2209ce19ecbcd8fecfb9e7d34fb4ee74 and manufactured by FUJIFILM medwork GmbH. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN 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