"Jingfang" Manual instruments for general surgery (unsterilized)
- Analysis ID
- 7ed8e61e27a5e805b78d9999543dc813
- Customs Code
- DHA09600444903
- Manufacturer Country
- China
- Authorized Representative
- LELTEK INC.
- Intended Use
- Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Chinese goods;; input
- Registration Date
- Feb 26, 2021
- Expiry Date
- Feb 26, 2026
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Access comprehensive regulatory information for "Jingfang" Manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7ed8e61e27a5e805b78d9999543dc813 and manufactured by JINGFANG PRECISION MEDICAL DEVICE (SHENZHEN) CO., LTD.. The authorized representative in Taiwan is LELTEK INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including JINGFANG PRECISION MEDICAL DEVICE (SHENZHEN) CO., LTD., and 1 recent registrations in the same category. 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.