Taiwan FDA registration b291b273c4e77d93daa4ea346265da40

"HEIWA" Manual surgical instrument for general use (Non-Sterile)

TW: "喜渥" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·HEIWA MEDICAL INSTRUMENTS CO., LTD.·Registered Jun 02, 2017 – Jun 02, 2027Active

Registration details

Analysis ID: b291b273c4e77d93daa4ea346265da40
License Form: Ministry of Health Medical Device Import No. 017908
Customs Code: DHA09401790801

Company information

Manufacturer: HEIWA MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: Japan
Authorized Representative: HEALTH RIVER INC.

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: Jun 02, 2017
Expiry Date: Jun 02, 2027

About this record

Access comprehensive regulatory information for "HEIWA" 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 b291b273c4e77d93daa4ea346265da40 and manufactured by HEIWA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HEALTH RIVER INC..

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