Taiwan FDA registration 203f338f0aef01d6d32075419f71f87a

"Apricot Whole" blood lancet (sterilized)

TW: "杏全" 採血針 (滅菌)

Taiwan·Risk Class 1·GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.·Registered Jan 03, 2013 – Jan 03, 2023Expired

Registration details

Analysis ID: 203f338f0aef01d6d32075419f71f87a
Customs Code: DHA04600181701

Company information

Manufacturer: GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.
Manufacturer Country: China
Authorized Representative: BEAM INTERNATIONAL 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: QMS/QSD;; Input;; Chinese goods

Dates and status

Registration Date: Jan 03, 2013
Expiry Date: Jan 03, 2023

About this record

Access comprehensive regulatory information for "Apricot Whole" blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 203f338f0aef01d6d32075419f71f87a and manufactured by GUANGZHOU IMPROVE MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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