"Synthes" Orthopedic Manual Surgical Instrument (NON-STERILE)
- Analysis ID
- 7b1e3dfd9f9eba0498861293d39b02fb
- License Form
- Ministry of Health Medical Device Import No. 015882
- Customs Code
- DHA09401588202
- Manufacturer
- SYNTHES (USA)
- Manufacturer Country
- United States
- Authorized Representative
- PRO-READY ENTERPRISE CO., LTD.
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N4540 Manual osteologic surgery instrument
- Import Information
- Imported from abroad
- Registration Date
- Nov 23, 2015
- Expiry Date
- Nov 23, 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 "Synthes" Orthopedic Manual Surgical Instrument (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 7b1e3dfd9f9eba0498861293d39b02fb and manufactured by SYNTHES (USA). The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including AVALIGN TECHNOLOGIES, 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.