Taiwan FDA registration 4c3625c68929eea5891e73650c889291
"Delang" inner lou tube wing needle
TW: “德朗”內婁管翼狀針
Taiwan·Risk Class 2·BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.·Registered Apr 25, 2011 – Apr 25, 2026ExpiredRegistration details
- Analysis ID
- 4c3625c68929eea5891e73650c889291
- Customs Code
- DHA04200030805
Company information
- Manufacturer
- BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- DORA MEDICAL EQUIPMENT CO., LTD.
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 25, 2011
- Expiry Date
- Apr 25, 2026
About this record
Access comprehensive regulatory information for "Delang" inner lou tube wing needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c3625c68929eea5891e73650c889291 and manufactured by BAIN MEDICAL EQUIPMENT (GUANGZHOU) CO., LTD.. The authorized representative in Taiwan is DORA MEDICAL EQUIPMENT CO., LTD..
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