Taiwan FDA registration 733cc56f4886e4f0f523a4df6b395a1b
"Digeio" is just the right time for the Nuoja Vitex electrostimulation electrotherapy system
TW: “帝傑歐”恰妥挪佳維生電刺激電療系統
Taiwan·Risk Class 2·DJO, LLC;; Verity Medical Ltd.·Registered Mar 23, 2017 – Mar 23, 2027ActiveRegistration details
- Analysis ID
- 733cc56f4886e4f0f523a4df6b395a1b
- Customs Code
- DHA05602942006
Company information
- Manufacturer
- DJO, LLC;; Verity Medical Ltd.
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- CONTINUOUS INSTRUMENT CO., LTD.
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
- Contract manufacturing;; input
Dates and status
- Registration Date
- Mar 23, 2017
- Expiry Date
- Mar 23, 2027
About this record
Access comprehensive regulatory information for "Digeio" is just the right time for the Nuoja Vitex electrostimulation electrotherapy system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 733cc56f4886e4f0f523a4df6b395a1b and manufactured by DJO, LLC;; Verity Medical Ltd.. The authorized representative in Taiwan is CONTINUOUS INSTRUMENT CO., LTD..
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