Taiwan FDA registration 21caf5f8bceb805acf3474b40c6ae8ba

"Snap Fai" Ligament Treatment Equipment (Non-Sterilized)

TW: "史耐輝" 韌帶處理設備(未滅菌)

Taiwan·Risk Class 1·ENZTEC LIMITED·Registered Jul 11, 2024 – Jul 11, 2029Active

Registration details

Analysis ID: 21caf5f8bceb805acf3474b40c6ae8ba
Customs Code: DHA09402353602

Company information

Manufacturer: ENZTEC LIMITED
Manufacturer Country: New Zealand
Authorized Representative: SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.)

Product details

Intended Use: It is limited to the first level of identification scope of manual orthopedic surgical instruments (N.4540) in the management measures for the classification and grading of medical devices.
Product Type (Level 1): N Orthopedics
Product Type (Level 2): N.4540 手動式骨科手術器械
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jul 11, 2024
Expiry Date: Jul 11, 2029

About this record

Access comprehensive regulatory information for "Snap Fai" Ligament Treatment Equipment (Non-Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 21caf5f8bceb805acf3474b40c6ae8ba and manufactured by ENZTEC LIMITED. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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