Taiwan FDA registration 4157cdf61650c1c1465d1753f7e98a58
Nipro GM-30 Inflation Device
TW: 尼普洛基曼擴張裝置
Taiwan·Risk Class 2·MD·GOODMAN CO., LTD. GOODMAN RESEARCH CENTER·Registered Mar 04, 2021 – Mar 04, 2026ExpiredRegistration details
- Analysis ID
- 4157cdf61650c1c1465d1753f7e98a58
- License Form
- Ministry of Health Medical Device Import No. 034348
- Customs Code
- DHA05603434805
Company information
- Manufacturer
- GOODMAN CO., LTD. GOODMAN RESEARCH CENTER
- Manufacturer Country
- Japan
- Authorized Representative
- LEIN YIH MEDICAL CO.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E1650 Vascular photography syringes and syringes
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 04, 2021
- Expiry Date
- Mar 04, 2026
About this record
Access comprehensive regulatory information for Nipro GM-30 Inflation Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4157cdf61650c1c1465d1753f7e98a58 and manufactured by GOODMAN CO., LTD. GOODMAN RESEARCH CENTER. The authorized representative in Taiwan is LEIN YIH MEDICAL CO..
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