Taiwan FDA registration af64707a621bc63389c5738ecab4ddac
AIRIP Medical Cold Pack (Unsterilized)
TW: 艾銳普 醫療用冷敷包 (未滅菌)
Taiwan·Risk Class 1·I-REP Therapy Products, Inc.·Registered Sep 02, 2022 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- af64707a621bc63389c5738ecab4ddac
- Customs Code
- DHA084a0010501
Company information
- Manufacturer
- I-REP Therapy Products, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- TISSUKINE CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5700 醫療用冷熱敷裝置
Dates and status
- Registration Date
- Sep 02, 2022
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for AIRIP Medical Cold Pack (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af64707a621bc63389c5738ecab4ddac and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is TISSUKINE CO., LTD..
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