Taiwan FDA registration 8588f8f53084a83341a87d47c33619bb
“UNIMAX” Anti-Fog Solution (Sterile)
TW: “普威”腹腔鏡用防霧油(滅菌)
Taiwan·Risk Class 2·MD·Puwei International Co., Ltd. Yilan Factory·Registered Dec 08, 2019 – Dec 08, 2024ExpiredRegistration details
- Analysis ID
- 8588f8f53084a83341a87d47c33619bb
- License Form
- Ministry of Health Medical Device Manufacturing No. 006651
Company information
- Manufacturer
- Puwei International Co., Ltd. Yilan Factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- UNIMAX MEDICAL SYSTEMS INC.
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)
- H1500 endoscope and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 08, 2019
- Expiry Date
- Dec 08, 2024
About this record
Access comprehensive regulatory information for “UNIMAX” Anti-Fog Solution (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8588f8f53084a83341a87d47c33619bb and manufactured by Puwei International Co., Ltd. Yilan Factory. The authorized representative in Taiwan is UNIMAX MEDICAL SYSTEMS INC..
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices