"FREEMAN" Limb orthosis (Non-Sterile)
Taiwan·Risk Class 1·MD·FREEMAN MANUFACTURING CO.·Registered Oct 29, 2015 – Oct 29, 2020Cancelled- Analysis ID
- 3dd2ec0a426059facce5f7b66a1ea1ea
- License Form
- Ministry of Health Medical Device Import No. 015797
- Customs Code
- DHA09401579708
- Manufacturer
- FREEMAN MANUFACTURING CO.
- Manufacturer Country
- United States
- Authorized Representative
- INNOVATIVE HEALTHCARE LTD.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Imported from abroad
- Registration Date
- Oct 29, 2015
- Expiry Date
- Oct 29, 2020
- Cancellation Date
- Jun 16, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
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Access comprehensive regulatory information for "FREEMAN" Limb orthosis (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3dd2ec0a426059facce5f7b66a1ea1ea and manufactured by FREEMAN MANUFACTURING CO.. The authorized representative in Taiwan is INNOVATIVE HEALTHCARE LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FREEMAN MANUFACTURING CO., and 2 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.