Taiwan FDA registration 323860f18725e3889934f611842855ca
"Nanxiang" manual osteologic surgical instrument (unsterilized)
TW: "南翔" 手動式骨科手術器械 (未滅菌)
Taiwan·Risk Class 1·Changzhou Nanxiang Medical Device Co., Ltd.·Registered Nov 30, 2022 – Nov 30, 2027ActiveRegistration details
- Analysis ID
- 323860f18725e3889934f611842855ca
- Customs Code
- DHA09600470406
Company information
- Manufacturer
- Changzhou Nanxiang Medical Device Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- PAONAN BIOTECH CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Manual orthopedic surgical instruments (N.4540)" first grade identification range.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.4540 手動式骨科手術器械
- Import Information
- Chinese goods;; Input;; QMS/QSD
Dates and status
- Registration Date
- Nov 30, 2022
- Expiry Date
- Nov 30, 2027
About this record
Access comprehensive regulatory information for "Nanxiang" manual osteologic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 323860f18725e3889934f611842855ca and manufactured by Changzhou Nanxiang Medical Device Co., Ltd.. The authorized representative in Taiwan is PAONAN BIOTECH CO., 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