Taiwan FDA registration 8c6de3aee288dcfc9655747d2866f387

"Mani" surgical suture needle (unsterilized)

TW: "馬尼" 外科用縫合針 (未滅菌)

Taiwan·Risk Class 1·MANI INC.;; MANI HANOI CO., LTD. PHO YEN 2 FACTORY·Registered Aug 01, 2019 – Aug 01, 2029Active

Registration details

Analysis ID: 8c6de3aee288dcfc9655747d2866f387
Customs Code: DHA09402070803

Company information

Manufacturer: MANI INC.;; MANI HANOI CO., LTD. PHO YEN 2 FACTORY
Manufacturer Country: Viet Nam;;Japan
Authorized Representative: UNIK SURGICAL SUTURES MFG. CO.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Contract manufacturing;; input

Dates and status

Registration Date: Aug 01, 2019
Expiry Date: Aug 01, 2029

About this record

Access comprehensive regulatory information for "Mani" surgical suture needle (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8c6de3aee288dcfc9655747d2866f387 and manufactured by MANI INC.;; MANI HANOI CO., LTD. PHO YEN 2 FACTORY. The authorized representative in Taiwan is UNIK SURGICAL SUTURES MFG. CO..

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