Taiwan FDA registration 2e485d0b2aa8cf6bea85dec21454a641

"SANRITU" Manual Surgical Instrument for General Use (Non-Sterile)

TW: "三立兹" 一般手術用手動式器械 (未滅菌)

Taiwan·Risk Class 1·MD·SANRITU MEDICAL INSTRUMENTS MFG. CO. LTD.·Registered Nov 19, 2013 – Nov 19, 2018Cancelled

Registration details

Analysis ID: 2e485d0b2aa8cf6bea85dec21454a641
License Form: Ministry of Health Medical Device Import No. 013599
Customs Code: DHA09401359907

Company information

Manufacturer: SANRITU MEDICAL INSTRUMENTS MFG. CO. LTD.
Manufacturer Country: Japan
Authorized Representative: MIN SHIN INSTRUMENTS CO., LTD.

Product details

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 19, 2013
Expiry Date: Nov 19, 2018
Cancellation Date: Jun 07, 2022

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "SANRITU" 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 2e485d0b2aa8cf6bea85dec21454a641 and manufactured by SANRITU MEDICAL INSTRUMENTS MFG. CO. LTD.. The authorized representative in Taiwan is MIN SHIN INSTRUMENTS CO., LTD..

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