Taiwan FDA registration 46002cbd2a3461743a44dd25afe21a27
“FINEMEDIX” Single-Use Clear-Hemostat Coagulation Probe
TW: “汎美德斯”單次用凝血探頭
Taiwan·Risk Class 2·MD·FINEMEDIX CO., LTD·Registered May 05, 2020 – May 05, 2025ExpiredRegistration details
- Analysis ID
- 46002cbd2a3461743a44dd25afe21a27
- License Form
- Ministry of Health Medical Device Import No. 033622
- Customs Code
- DHA05603362207
Company information
- Manufacturer
- FINEMEDIX CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- SCHMIDT SCIENTIFIC TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H4300 Electrocutors for endoscopes and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 05, 2020
- Expiry Date
- May 05, 2025
About this record
Access comprehensive regulatory information for “FINEMEDIX” Single-Use Clear-Hemostat Coagulation Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46002cbd2a3461743a44dd25afe21a27 and manufactured by FINEMEDIX CO., LTD. The authorized representative in Taiwan is SCHMIDT SCIENTIFIC TAIWAN LTD..
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