“PENTAX” ELECTRO-SURGICAL KNIFE
Taiwan·Risk Class 2·MD·HOYA CORPORATION PENTAX YAMAGATA FACTORY·Registered May 10, 2016 – May 10, 2026Expired- Analysis ID
- e9606cc25b5d0e9f467086a6bb7e369c
- License Form
- Ministry of Health Medical Device Import No. 028572
- Customs Code
- DHA05602857201
- Manufacturer
- HOYA CORPORATION PENTAX YAMAGATA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE)
- 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
- Registration Date
- May 10, 2016
- Expiry Date
- May 10, 2026
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Access comprehensive regulatory information for “PENTAX” ELECTRO-SURGICAL KNIFE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e9606cc25b5d0e9f467086a6bb7e369c and manufactured by HOYA CORPORATION PENTAX YAMAGATA FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA CORPORATION PENTAX YAMAGATA FACTORY, 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.