Taiwan FDA registration 4891ce5e40d72060fc90180663f0117e
“Lumenis” VersaCut Morcellator System
TW: “洛明尼斯”組織粉碎系統
Taiwan·Risk Class 2·MD·LUMENIS LTD.·Registered Aug 16, 2017 – Aug 16, 2027ActiveRegistration details
- Analysis ID
- 4891ce5e40d72060fc90180663f0117e
- License Form
- Ministry of Health Medical Device Import No. 030115
- Customs Code
- DHA05603011501
Company information
- Manufacturer
- LUMENIS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS)
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 16, 2017
- Expiry Date
- Aug 16, 2027
About this record
Access comprehensive regulatory information for “Lumenis” VersaCut Morcellator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4891ce5e40d72060fc90180663f0117e and manufactured by LUMENIS LTD.. The authorized representative in Taiwan is BOSTON SCIENTIFIC INTERNATIONAL B.V., TAIWAN BRANCH (NETHERLANDS).
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