Taiwan FDA registration 49db053f5981d5f22865579694d99fa6
“BAIHE” Disposable Silicone Foley Catheter
TW: “百合”矽質導尿管
Taiwan·Risk Class 2·MD·GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.·Registered Apr 18, 2014 – Apr 18, 2024ExpiredRegistration details
- Analysis ID
- 49db053f5981d5f22865579694d99fa6
- License Form
- Ministry of Health Medical Device Land Transport No. 000603
- Customs Code
- DHA09200060300
Company information
- Manufacturer
- GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HURRAYBIO 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)
- H5130 Urinary catheters and their accessories
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Apr 18, 2014
- Expiry Date
- Apr 18, 2024
About this record
Access comprehensive regulatory information for “BAIHE” Disposable Silicone Foley Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 49db053f5981d5f22865579694d99fa6 and manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HURRAYBIO CO., LTD..
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