Taiwan FDA registration c5018a9df2423bba52064f97f2b5fcde

"BROSS" Manual surgical instrument for general use (NON-STERILE)

TW: "柏斯" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·BROSS MEDICAL GMBH·Registered Nov 11, 2016 – Nov 11, 2021Expired

Registration details

Analysis ID: c5018a9df2423bba52064f97f2b5fcde
License Form: Ministry of Health Medical Device Import No. 017172
Customs Code: DHA09401717204

Company information

Manufacturer: BROSS MEDICAL GMBH
Manufacturer Country: Germany
Authorized Representative: PRO-READY ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4800 General Surgery Manual Instrument
Import Information: Imported from abroad

Dates and status

Registration Date: Nov 11, 2016
Expiry Date: Nov 11, 2021

About this record

Access comprehensive regulatory information for "BROSS" Manual surgical instrument for general use (NON-STERILE) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c5018a9df2423bba52064f97f2b5fcde and manufactured by BROSS MEDICAL GMBH. The authorized representative in Taiwan is PRO-READY ENTERPRISE CO., LTD..

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