Taiwan FDA registration e94502b2230bbde3ff9d174af8b72a9a
"Erip" medical cold compress pack (unsterilized)
TW: "艾瑞普"醫療用冷敷包(未滅菌)
Taiwan·Risk Class 1·I-REP Therapy Products, Inc.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- e94502b2230bbde3ff9d174af8b72a9a
- Customs Code
- DHA08401489609
Company information
- Manufacturer
- I-REP Therapy Products, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ORTHOHEALTH 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
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
- Cancellation Date
- Nov 21, 2024
About this record
Access comprehensive regulatory information for "Erip" medical cold compress 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 e94502b2230bbde3ff9d174af8b72a9a and manufactured by I-REP Therapy Products, Inc.. The authorized representative in Taiwan is ORTHOHEALTH CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices