Taiwan FDA registration ceeb3faf37f9347d63286b75bf79156a
"I.V. House" TLC UltraSplint (Non-Sterile)
TW: "愛伏護" 固定板 (未滅菌)
Taiwan·Risk Class 1·MD·I.V. HOUSE, INC.·Registered Feb 05, 2016 – Feb 05, 2021ExpiredRegistration details
- Analysis ID
- ceeb3faf37f9347d63286b75bf79156a
- License Form
- Ministry of Health Medical Device Import No. 016153
- Customs Code
- DHA09401615308
Company information
- Manufacturer
- I.V. HOUSE, INC.
- Manufacturer Country
- United States
- Authorized Representative
- MIMED CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Splints for Non-Expanded Limbs (I.3910)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I3910 Splints for non-inflated extremities
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 05, 2016
- Expiry Date
- Feb 05, 2021
About this record
Access comprehensive regulatory information for "I.V. House" TLC UltraSplint (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 ceeb3faf37f9347d63286b75bf79156a and manufactured by I.V. HOUSE, INC.. The authorized representative in Taiwan is MIMED CO., LTD..
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