Taiwan FDA registration b9d7539022d99e6ed1537b3a8cdcdae9

"Enrif" muscle stimulator

TW: “恩瑞福”肌肉刺激器
Taiwan flagTaiwan·Risk Class 2·ENRAF-NONIUS B.V.;; AIM B.V.·Registered Nov 23, 2012 – Nov 23, 2022Cancelled
Registration details
Analysis ID
b9d7539022d99e6ed1537b3a8cdcdae9
Customs Code
DHA00602418201
Company information
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
Input;; Contract manufacturing
Dates and status
Registration Date
Nov 23, 2012
Expiry Date
Nov 23, 2022
Cancellation Date
Apr 12, 2024
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
About this record

Access comprehensive regulatory information for "Enrif" muscle stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b9d7539022d99e6ed1537b3a8cdcdae9 and manufactured by ENRAF-NONIUS B.V.;; AIM 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