Taiwan FDA registration e0eb344ac78e70f3ba6c20f32738757d

Tenderlett Finger Incision Device (Sterile)

TW: 疼得樂指尖劃割式採血器(滅菌)

Taiwan·Risk Class 1·MD·Accriva (dba) International Technidyne Corporation (ITC) (dba) Accumetrics·Registered Jan 08, 2018 – Jan 08, 2023Expired

Registration details

Analysis ID: e0eb344ac78e70f3ba6c20f32738757d
License Form: Ministry of Health Medical Device Import No. 018699
Customs Code: DHA09401869900

Company information

Manufacturer: Accriva (dba) International Technidyne Corporation (ITC) (dba) Accumetrics
Manufacturer Country: United States
Authorized Representative: BioChain 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: Jan 08, 2018
Expiry Date: Jan 08, 2023

About this record

Access comprehensive regulatory information for Tenderlett Finger Incision Device (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e0eb344ac78e70f3ba6c20f32738757d and manufactured by Accriva (dba) International Technidyne Corporation (ITC) (dba) Accumetrics. The authorized representative in Taiwan is BioChain Co., Ltd..

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