"A.P" Manual surgical instrument for general use (non-sterile)
Taiwan·Risk Class 1·MD·A.P MEDICAL·Registered Nov 15, 2013 – Nov 15, 2018Cancelled- Analysis ID
- ba07da3427b15d85fcc0f80a02cdb74e
- License Form
- Ministry of Health Medical Device Import No. 013595
- Customs Code
- DHA09401359502
- Manufacturer
- A.P MEDICAL
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- PRIMESTAR MEDICAL CO., LTD.
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
- Registration Date
- Nov 15, 2013
- Expiry Date
- Nov 15, 2018
- 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 "A.P" Manual surgical instrument for general use (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 ba07da3427b15d85fcc0f80a02cdb74e and manufactured by A.P MEDICAL. The authorized representative in Taiwan is PRIMESTAR MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including A.P MEDICAL, 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.