Taiwan FDA registration a300c1e49be4056f43843abaa014aab0

"Conwilli" Splint for inflated extremities (unsterilized)

TW: "康威利" 膨脹式四肢用夾板 (未滅菌)

Taiwan·Risk Class 1·CONWELL MEDICAL CO., LTD.·Registered Jun 20, 2016 – Jun 20, 2026Expired

Registration details

Analysis ID: a300c1e49be4056f43843abaa014aab0

Company information

Manufacturer: CONWELL MEDICAL CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CONWELL MEDICAL CO., LTD.

Product details

Intended Use: It is limited to the first level identification scope of the splint for inflatable limbs (I.3900) in the classification and grading management measures for medical equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.3900 Clamp board for bulging limbs
Import Information: Domestic

Dates and status

Registration Date: Jun 20, 2016
Expiry Date: Jun 20, 2026

About this record

Access comprehensive regulatory information for "Conwilli" Splint for inflated extremities (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a300c1e49be4056f43843abaa014aab0 and manufactured by CONWELL MEDICAL CO., LTD.. The authorized representative in Taiwan is CONWELL MEDICAL CO., LTD..

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