Taiwan FDA registration d3a5b2b772cc0947bbdd07f764815824
“Veol” VERSATOR Tissue Morcellation System
TW: “威爾”組織切除系統
Taiwan·Risk Class 2·MD·Veol Medical Technologies Pvt. Ltd.·Registered Jul 16, 2020 – Jul 16, 2025ExpiredRegistration details
- Analysis ID
- d3a5b2b772cc0947bbdd07f764815824
- License Form
- Ministry of Health Medical Device Import No. 033795
- Customs Code
- DHA05603379502
Company information
- Manufacturer
- Veol Medical Technologies Pvt. Ltd.
- Manufacturer Country
- India
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- l Devices for obstetrics and gynecology
- Product Type (Level 2)
- L1720 Laparoscopy for obstetrics and gynecology and its accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 16, 2020
- Expiry Date
- Jul 16, 2025
About this record
Access comprehensive regulatory information for “Veol” VERSATOR Tissue 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 d3a5b2b772cc0947bbdd07f764815824 and manufactured by Veol Medical Technologies Pvt. Ltd.. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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