Taiwan FDA registration 7528524f94b85b0a8f0020dbf53300ff
“O.R.” McCartney/ColpotomizOR Tube
TW: “歐爾”經陰道手術套管
Taiwan·Risk Class 2·MD·The OR Company Pty Ltd·Registered Aug 20, 2020 – Aug 20, 2025ExpiredRegistration details
- Analysis ID
- 7528524f94b85b0a8f0020dbf53300ff
- License Form
- Ministry of Health Medical Device Import No. 033893
- Customs Code
- DHA05603389302
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
- Aug 20, 2020
- Expiry Date
- Aug 20, 2025
About this record
Access comprehensive regulatory information for “O.R.” McCartney/ColpotomizOR Tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7528524f94b85b0a8f0020dbf53300ff and manufactured by The OR Company Pty Ltd. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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