Taiwan FDA registration 19698c3e951a86070a0a5ff65253e4d6
“JenaSurgical” MulitCut Solo Morcellation System
TW: “捷納外科”粉碎器系統
Registration details
- Analysis ID
- 19698c3e951a86070a0a5ff65253e4d6
- License Form
- Ministry of Health Medical Device Import No. 035577
- Customs Code
- DHA05603557702
Company information
- Manufacturer
- Asclepion Laser Technologies GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- JIANHE BIO-MEDICAL 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)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 10, 2022
- Expiry Date
- Jun 10, 2027
About this record
Access comprehensive regulatory information for “JenaSurgical” MulitCut Solo Morcellation System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 19698c3e951a86070a0a5ff65253e4d6 and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is JIANHE BIO-MEDICAL 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