Taiwan FDA registration 67cf3e46f912233a34bf6306288ccff9

"A.R.C." Manual Surgical Instrument for General Use (Non-Sterile)

TW: "艾爾皙" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·A.R.C. LASER GMBH·Registered Oct 15, 2018 – Oct 15, 2023Expired

Registration details

Analysis ID: 67cf3e46f912233a34bf6306288ccff9
License Form: Ministry of Health Medical Device Import No. 019703
Customs Code: DHA09401970306

Company information

Manufacturer: A.R.C. LASER GMBH
Manufacturer Country: Germany
Authorized Representative: Winrise Medical 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: Oct 15, 2018
Expiry Date: Oct 15, 2023

About this record

Access comprehensive regulatory information for "A.R.C." 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 67cf3e46f912233a34bf6306288ccff9 and manufactured by A.R.C. LASER GMBH. The authorized representative in Taiwan is Winrise Medical Co., Ltd..

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