Taiwan FDA registration 26c2a1532a316f1a640f3ac9575bbbe1
"Chang'an" lumbar intervertebral implant
TW: "長安"腰椎椎間植入物
Taiwan·Risk Class 2·WELLONG INSTRUMENTS CO., LTD.·Registered Oct 30, 2007 – Oct 30, 2027ActiveRegistration details
- Analysis ID
- 26c2a1532a316f1a640f3ac9575bbbe1
- Customs Code
- DHY00500236608
Company information
- Manufacturer
- WELLONG INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WELLONG INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3060 椎體間之脊椎矯正固定物
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 30, 2007
- Expiry Date
- Oct 30, 2027
About this record
Access comprehensive regulatory information for "Chang'an" lumbar intervertebral implant in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 26c2a1532a316f1a640f3ac9575bbbe1 and manufactured by WELLONG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is WELLONG INSTRUMENTS CO., LTD..
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