Johnson & Johnson in vitro prosthetic components (unsterilized)
- Analysis ID
- 1a1fc0a73a202633935825720021cec0
- Customs Code
- DHA08400695302
- Manufacturer
- FRIDDLE "S ORTHOPEDIC APPLIANCES
- Manufacturer Country
- United States
- Authorized Representative
- JOHNSON A. L. TRADING CO., LTD.
- Intended Use
- Limited to the classification and grading management method of medical equipment, in vitro limb prosthetic components (O.3420) the first level recognition range.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3420 體外肢體義肢用組件
- Import Information
- import
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
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Access comprehensive regulatory information for Johnson & Johnson in vitro prosthetic components (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1a1fc0a73a202633935825720021cec0 and manufactured by FRIDDLE "S ORTHOPEDIC APPLIANCES. The authorized representative in Taiwan is JOHNSON A. L. TRADING CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including BLATCHFORD PRODUCTS LTD., PEL SUPPLY CO., and 5 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.