Taiwan FDA registration ff83cf5af87186bdf01ad1224b5e3140
"Unified" new resin fiber pre-module (unsterilized)
TW: "統合" 新型樹脂纖維預模組 (未滅菌)
Taiwan·Risk Class 1·DONG HAE MEDICAL CO., LTD·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- ff83cf5af87186bdf01ad1224b5e3140
- Customs Code
- DHA08401785000
Company information
- Manufacturer
- DONG HAE MEDICAL CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- GREAT KUEI TAI INC.
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 "Unified" new resin fiber pre-module (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff83cf5af87186bdf01ad1224b5e3140 and manufactured by DONG HAE MEDICAL CO., LTD. The authorized representative in Taiwan is GREAT KUEI TAI INC..
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