Taiwan FDA registration 8845c637c076c2c42597bb372fd24568
“ENGAIN” EGgel Gelatin Microparticles Embolization Agent
TW: “伊格”明膠微粒栓塞物
Registration details
- Analysis ID
- 8845c637c076c2c42597bb372fd24568
- License Form
- Ministry of Health Medical Device Import No. 033892
- Customs Code
- DHA05603389200
Company information
- Manufacturer
- ENGAIN Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- Yuantech International Co, Ltd.
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)
- E3300 Arterial Embolization Device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 20, 2020
- Expiry Date
- Aug 20, 2025
About this record
Access comprehensive regulatory information for “ENGAIN” EGgel Gelatin Microparticles Embolization Agent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8845c637c076c2c42597bb372fd24568 and manufactured by ENGAIN Co., Ltd.. The authorized representative in Taiwan is Yuantech International 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