Taiwan FDA registration f60020d7cc34a5f8e49e1c0a5b501689
"Baonan" Lockma interridge decompression system
TW: “寶楠”洛克馬脊突間減壓系統
Taiwan·Risk Class 2·PAONAN BIOTECH CO., LTD.·Registered Apr 10, 2013 – Apr 10, 2028ActiveRegistration details
- Analysis ID
- f60020d7cc34a5f8e49e1c0a5b501689
Company information
- Manufacturer
- PAONAN BIOTECH CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- PAONAN BIOTECH 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.3050 椎弓板間之脊椎矯正固定物
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 10, 2013
- Expiry Date
- Apr 10, 2028
About this record
Access comprehensive regulatory information for "Baonan" Lockma interridge decompression system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f60020d7cc34a5f8e49e1c0a5b501689 and manufactured by PAONAN BIOTECH CO., LTD.. The authorized representative in Taiwan is PAONAN BIOTECH 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