Taiwan FDA registration 88a6b37ccfd31eb49989d63b8dcdc688
Cement Spacer Mold
TW: “聯合”骨水泥髖關節塑模
Taiwan·Risk Class 2·MD·UNITED ORTHOPEDIC CORPORATION·Registered Sep 05, 2017 – Sep 05, 2027ActiveRegistration details
- Analysis ID
- 88a6b37ccfd31eb49989d63b8dcdc688
- License Form
- Ministry of Health Medical Device Manufacturing No. 005900
Company information
- Manufacturer
- UNITED ORTHOPEDIC CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNITED ORTHOPEDIC CORPORATION
Product details
- Intended Use
- This product is suitable for shaping temporary femoral implants.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3360 Hip femur (semi-hip) metal cement or cementless type compound
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Sep 05, 2017
- Expiry Date
- Sep 05, 2027
About this record
Access comprehensive regulatory information for Cement Spacer Mold in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 88a6b37ccfd31eb49989d63b8dcdc688 and manufactured by UNITED ORTHOPEDIC CORPORATION. The authorized representative in Taiwan is UNITED ORTHOPEDIC CORPORATION.
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