"Martin" Cardiovascular Surgical Instruments (Non-Sterile)
Taiwan·Risk Class 1·MD·GEBRUEDER MARTIN GMBH & CO. KG·Registered Sep 16, 2013 – Sep 16, 2018Cancelled- Analysis ID
- f8349fcf97df7ee0bbdbc177b3e95fb1
- License Form
- Ministry of Health Medical Device Import No. 013429
- Customs Code
- DHA09401342908
- Manufacturer
- GEBRUEDER MARTIN GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- KINDMED CORPORATION
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E4500 Cardiovascular Surgical Instrument
- Import Information
- Imported from abroad
- Registration Date
- Sep 16, 2013
- Expiry Date
- Sep 16, 2018
- Cancellation Date
- Aug 05, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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Access comprehensive regulatory information for "Martin" Cardiovascular Surgical Instruments (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 f8349fcf97df7ee0bbdbc177b3e95fb1 and manufactured by GEBRUEDER MARTIN GMBH & CO. KG. The authorized representative in Taiwan is KINDMED CORPORATION.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GEBRUEDER MARTIN GMBH & CO. KG, 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.