Taiwan FDA registration ba0b4d26402213b0978dc3d6b606c658
"Rudolf" General Surgical Instruments (Non-Sterile)
TW: "魯道夫" 一般手術器械 (未滅菌)
Taiwan·Risk Class 1·MD·RUDOLF MEDICAL GMBH & CO. KG·Registered Jan 06, 2016 – Jan 06, 2026ExpiredRegistration details
- Analysis ID
- ba0b4d26402213b0978dc3d6b606c658
- License Form
- Ministry of Health Medical Device Import No. 016054
- Customs Code
- DHA09401605406
Company information
- Manufacturer
- RUDOLF MEDICAL GMBH & CO. KG
- Manufacturer Country
- Germany
- Authorized Representative
- JAU SHAUNN INSTRUMENT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I4800 General Surgery Manual Instrument
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 06, 2016
- Expiry Date
- Jan 06, 2026
About this record
Access comprehensive regulatory information for "Rudolf" General Surgical Instruments (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ba0b4d26402213b0978dc3d6b606c658 and manufactured by RUDOLF MEDICAL GMBH & CO. KG. The authorized representative in Taiwan is JAU SHAUNN INSTRUMENT 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