Taiwan FDA registration e4c645e79663c21df261d712ae33bfdb
"Enrif" electrotherapy device
TW: “恩瑞福”電療治療器
Taiwan·Risk Class 2·ENRAF-NONIUS B.V.·Registered Jun 18, 2008 – Jun 18, 2023ExpiredRegistration details
- Analysis ID
- e4c645e79663c21df261d712ae33bfdb
- Customs Code
- DHA00601891108
Company information
- Manufacturer
- ENRAF-NONIUS B.V.
- Manufacturer Country
- Netherlands
- Authorized Representative
- GOOD LINE INCORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5850 5850.
- Import Information
- import
Dates and status
- Registration Date
- Jun 18, 2008
- Expiry Date
- Jun 18, 2023
About this record
Access comprehensive regulatory information for "Enrif" electrotherapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e4c645e79663c21df261d712ae33bfdb and manufactured by ENRAF-NONIUS B.V.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
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