Taiwan FDA registration 0b3500cbbd8e30abb43dad00cb84ef94
“KDL” Disposable Spinal Needle
TW: “康德萊”一次性使用麻醉針
Taiwan·Risk Class 2·MD·Zhejiang Kindly Medical Devices Co., Ltd.·Registered Feb 14, 2014 – Feb 14, 2024ExpiredRegistration details
- Analysis ID
- 0b3500cbbd8e30abb43dad00cb84ef94
- License Form
- Ministry of Health Medical Device Land Transport No. 000576
- Customs Code
- DHA09200057600
Company information
- Manufacturer
- Zhejiang Kindly Medical Devices Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- KENYEN INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5150 Anesthesia Transfer Needle
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Feb 14, 2014
- Expiry Date
- Feb 14, 2024
About this record
Access comprehensive regulatory information for “KDL” Disposable Spinal Needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0b3500cbbd8e30abb43dad00cb84ef94 and manufactured by Zhejiang Kindly Medical Devices Co., Ltd.. The authorized representative in Taiwan is KENYEN INTERNATIONAL INC..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices