Taiwan FDA registration 14f725547492cd6b22c25b31a209ba46
"Xingchang" blood circuit tube
TW: “杏昌”血液迴路管
Taiwan·Risk Class 2·BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.·Registered Apr 26, 2012 – Apr 26, 2027ActiveRegistration details
- Analysis ID
- 14f725547492cd6b22c25b31a209ba46
- Customs Code
- DHA04200043907
Company information
- Manufacturer
- BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- HI-CLEARANCE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5540 Blood Access Devices and Accessories
- Import Information
- Chinese goods;; input
Dates and status
- Registration Date
- Apr 26, 2012
- Expiry Date
- Apr 26, 2027
About this record
Access comprehensive regulatory information for "Xingchang" blood circuit tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 14f725547492cd6b22c25b31a209ba46 and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is HI-CLEARANCE INC..
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