Taiwan FDA registration d7c0dd9545751b2ccc0f80f35a7d30a1

"Ausheng" surgical headlamp (unsterilized)

TW: "奧盛" 手術用頭燈(未滅菌)

Taiwan·Risk Class 1·ALLTION (GUANGXI) INSTRUMENT CO., LTD.·Registered Nov 07, 2022 – Nov 07, 2027Active

Registration details

Analysis ID: d7c0dd9545751b2ccc0f80f35a7d30a1
Customs Code: DHA09600469008

Company information

Manufacturer: ALLTION (GUANGXI) INSTRUMENT CO., LTD.
Manufacturer Country: China
Authorized Representative: Zenpe-medical Co., Ltd.

Product details

Intended Use: Limited to the classification and grading management measures of medical equipment "Surgical Headlamp (M.4335)" first level identification range.
Product Type (Level 1): M Ophthalmology
Product Type (Level 2): M.4335 Headlamps for surgery
Import Information: Input;; Chinese goods

Dates and status

Registration Date: Nov 07, 2022
Expiry Date: Nov 07, 2027

About this record

Access comprehensive regulatory information for "Ausheng" surgical headlamp (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7c0dd9545751b2ccc0f80f35a7d30a1 and manufactured by ALLTION (GUANGXI) INSTRUMENT CO., LTD.. The authorized representative in Taiwan is Zenpe-medical Co., Ltd..

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