Taiwan FDA registration e78488f61be05d5daa4ef5d9daf4512f

BD Snowden Pencer Retractor (Non-Sterile)

TW: BD 牽引器(未滅菌)

Taiwan·Risk Class 1·MD·CAREFUSION·Registered Sep 11, 2019 – Sep 11, 2024Expired

Registration details

Analysis ID: e78488f61be05d5daa4ef5d9daf4512f
License Form: Ministry of Health Medical Device Import No. 020847
Customs Code: DHA09402084704

Company information

Manufacturer: CAREFUSION
Manufacturer Country: United States
Authorized Representative: BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)

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: Sep 11, 2019
Expiry Date: Sep 11, 2024

About this record

Access comprehensive regulatory information for BD Snowden Pencer Retractor (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 e78488f61be05d5daa4ef5d9daf4512f and manufactured by CAREFUSION. The authorized representative in Taiwan is BECTON DICKINSON HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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