Taiwan FDA registration db0742ebd73e3c94ed2b838ad768bd76
"DJO" Cold Pack (Non-Sterile)
TW: "歐凱"醫療用冷敷包(未滅菌)
Taiwan·Risk Class 1·MD·DJO, LLC·Registered Jul 01, 2014 – Jul 01, 2019CancelledRegistration details
- Analysis ID
- db0742ebd73e3c94ed2b838ad768bd76
- License Form
- Ministry of Health Medical Device Import No. 014290
- Customs Code
- DHA09401429008
Company information
- Manufacturer
- DJO, LLC
- 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
- Jul 01, 2014
- Expiry Date
- Jul 01, 2019
- Cancellation Date
- Jun 07, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "DJO" 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 db0742ebd73e3c94ed2b838ad768bd76 and manufactured by DJO, LLC. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..
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