Taiwan FDA registration 72228ba48cb5fc0b114bd35d594152ff
“CIVCO”Gastroenterology-urology biopsy instrument(Sterile)
TW: “席弗科”腸胃科-泌尿科生檢器械 (滅菌)
Registration details
- Analysis ID
- 72228ba48cb5fc0b114bd35d594152ff
- License Form
- Ministry of Health Medical Device Import No. 013324
- Customs Code
- DHA09401332407
Company information
- Manufacturer
- CIVCO MEDICAL INSTRUMENTS CO., INC
- Manufacturer Country
- United States
- Authorized Representative
- CHINA SPRING TRADING CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Gastroenterology-Urology Bioexamination Devices (H.1075)".
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1075 Gastroenterology - Urology biopsy instruments
- Import Information
- Imported from abroad; GMP
Dates and status
- Registration Date
- Aug 22, 2013
- Expiry Date
- Aug 22, 2028
About this record
Access comprehensive regulatory information for “CIVCO”Gastroenterology-urology biopsy instrument(Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 72228ba48cb5fc0b114bd35d594152ff and manufactured by CIVCO MEDICAL INSTRUMENTS CO., INC. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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