Taiwan FDA registration c68774d2de1076e97a5b33faccf131fd
“O.R.” ColpotomizOR Tube System
TW: “歐爾”經陰道手術套管組
Taiwan·Risk Class 2·MD·The OR Company Pty Ltd·Registered Oct 12, 2020 – Oct 12, 2025ExpiredRegistration details
- Analysis ID
- c68774d2de1076e97a5b33faccf131fd
- License Form
- Ministry of Health Medical Device Import No. 033977
- Customs Code
- DHA05603397705
Company information
- Manufacturer
- The OR Company Pty Ltd
- Manufacturer Country
- Australia
- 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)
- L1640 recessed mirror and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 12, 2020
- Expiry Date
- Oct 12, 2025
About this record
Access comprehensive regulatory information for “O.R.” ColpotomizOR Tube System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c68774d2de1076e97a5b33faccf131fd and manufactured by The OR Company Pty Ltd. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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