Taiwan FDA registration 836012a4eba2663d4f9134c04345400d
"I-M" HERNIA SUPPORT (Non-Sterile)
TW: "愛民" 疝脫支撐器 (未滅菌)
Taiwan·Risk Class 1·MD·Aimin Eisai Co., Ltd. Plant 2·Registered Oct 01, 2021 – Oct 31, 2025CancelledRegistration details
- Analysis ID
- 836012a4eba2663d4f9134c04345400d
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 000089
- Customs Code
- DHY08300008902
Company information
- Manufacturer
- Aimin Eisai Co., Ltd. Plant 2
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Aimin Eisai Co., Ltd. Plant 2
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5970 Hernia Brace
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
- Cancellation Date
- Oct 28, 2022
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "I-M" HERNIA SUPPORT (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 836012a4eba2663d4f9134c04345400d and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is Aimin Eisai Co., Ltd. Plant 2.
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