Taiwan FDA registration dce03358524becca4e4a52e489a09ade
"I-REP" Cold Pack (Non-Sterile)
TW: "艾瑞普"醫療用冷敷包(未滅菌)
Taiwan·Risk Class 1·MD·I-REP Therapy Products, Inc.·Registered Jan 30, 2015 – Jan 30, 2025CancelledRegistration details
- Analysis ID
- dce03358524becca4e4a52e489a09ade
- License Form
- Ministry of Health Medical Device Import No. 014896
- Customs Code
- DHA09401489605
Company information
- Manufacturer
- I-REP Therapy Products, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ORTHOHEALTH CO., LTD.
Product details
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5700 Medical Cold Pack
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 30, 2015
- Expiry Date
- Jan 30, 2025
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for "I-REP" Cold Pack (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 dce03358524becca4e4a52e489a09ade and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..
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