Taiwan FDA registration f32142f8fd4ab121a57aeba33cdd1d1d
"Whitehall" Noninflatable extremity splint (Non-Sterile)
TW: "懷侯"非膨脹式四肢用夾板(未滅菌)
Taiwan·Risk Class 1·MD·WHITEHALL MANUFACTURING, INC.·Registered Oct 01, 2021 – Oct 31, 2026ActiveRegistration details
- Analysis ID
- f32142f8fd4ab121a57aeba33cdd1d1d
- License Form
- Ministry of Health Medical Device Import Registration No. 010397
- Customs Code
- DHA08401039700
Company information
- Manufacturer
- WHITEHALL MANUFACTURING, INC.
- Manufacturer Country
- United States
- Authorized Representative
- GOOD LINE INCORPORATION
Product details
- Intended Use
- Measures for the Administration of Medical Devices Limited" (.) The first level of identification range.
- 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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
About this record
Access comprehensive regulatory information for "Whitehall" Noninflatable extremity splint (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 f32142f8fd4ab121a57aeba33cdd1d1d and manufactured by WHITEHALL MANUFACTURING, INC.. The authorized representative in Taiwan is GOOD LINE INCORPORATION.
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