Taiwan FDA registration e4a23c0c6cfa382b7835163c358021fa
"Ellard" limb equipment (unsterilized)
TW: "艾拉德" 肢體裝具 (未滅菌)
Registration details
- Analysis ID
- e4a23c0c6cfa382b7835163c358021fa
- Customs Code
- DHA08401374601
Company information
- Manufacturer
- ALLARD USA INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHENG CHUAN P&O CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of medical equipment classification and grading management measures limb equipment (O.3475).
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.3475 Limb fittings
- Import Information
- import
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Ellard" limb equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e4a23c0c6cfa382b7835163c358021fa and manufactured by ALLARD USA INC.. The authorized representative in Taiwan is CHENG CHUAN P&O 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.
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