Taiwan FDA registration fce7523d75c5af5db409b9a4cdc1f2b7
"Enrif" ultrasound combined with electrodes and therapy device
TW: "恩瑞福" 超音波與電極合併治療器
Taiwan·Risk Class 2·ENRAF-NONIUS B.V.;; AIM B.V.·Registered Dec 27, 2004 – Dec 27, 2019CancelledRegistration details
- Analysis ID
- fce7523d75c5af5db409b9a4cdc1f2b7
- Customs Code
- DHA00601097902
Company information
- Manufacturer
- ENRAF-NONIUS B.V.;; AIM 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
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Dec 27, 2004
- Expiry Date
- Dec 27, 2019
- Cancellation Date
- Aug 05, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Enrif" ultrasound combined with electrodes and therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fce7523d75c5af5db409b9a4cdc1f2b7 and manufactured by ENRAF-NONIUS B.V.;; AIM B.V.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
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