Taiwan FDA registration 06d3a46060a6ced1ecf58e03d2719de6
“SUNDER” Endo Bag
TW: “善德”取物袋
Registration details
- Analysis ID
- 06d3a46060a6ced1ecf58e03d2719de6
- License Form
- Ministry of Health Medical Device Manufacturing No. 006905
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SUNDER BIOMEDICAL TECH. CO., LTD.
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
- Jun 24, 2020
- Expiry Date
- Jun 24, 2025
About this record
Access comprehensive regulatory information for “SUNDER” Endo Bag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 06d3a46060a6ced1ecf58e03d2719de6 and manufactured by Shande Biochemical Technology Co., Ltd. is loyal to the factory. The authorized representative in Taiwan is SUNDER BIOMEDICAL TECH. CO., LTD..
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