Taiwan FDA registration c962212e27f337702fc9f929bce71dd0
"Jie Yi" Manual Orthopedic Surgical Instruments (Sterilized/Unsterilized)
TW: "傑醫" 手動式骨科手術器械 (滅菌/未滅菌)
Taiwan·Risk Class 1·JOIMAX GMBH·Registered Oct 27, 2020 – Oct 27, 2025ExpiredRegistration details
- Analysis ID
- c962212e27f337702fc9f929bce71dd0
- Customs Code
- DHA09402206306
Company information
- Manufacturer
- JOIMAX GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- K&C MEDICAL 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
- Input;; QMS/QSD
Dates and status
- Registration Date
- Oct 27, 2020
- Expiry Date
- Oct 27, 2025
About this record
Access comprehensive regulatory information for "Jie Yi" Manual Orthopedic Surgical Instruments (Sterilized/Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c962212e27f337702fc9f929bce71dd0 and manufactured by JOIMAX GMBH. The authorized representative in Taiwan is K&C MEDICAL CO., LTD..
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