Taiwan FDA registration 8334302c78e8c997bd979c7351f51ce5

"De Anfang" Rollis Blood Collection Needle (Sterilized)

TW: 〝德安芳〞羅利士採血針 (滅菌)

Taiwan·Risk Class 1·LERNAPHARM INC.;; STERILANCE MEDICAL (SUZHOU) INC.·Registered Nov 09, 2011 – Nov 09, 2016Cancelled

Registration details

Analysis ID: 8334302c78e8c997bd979c7351f51ce5
Customs Code: DHA04600151001

Company information

Manufacturer: LERNAPHARM INC.;; STERILANCE MEDICAL (SUZHOU) INC.
Manufacturer Country: Canada;;China
Authorized Representative: U-E CHECK MEDICAL 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, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Contract manufacturing;; Input;; Chinese goods;; QMS/QSD

Dates and status

Registration Date: Nov 09, 2011
Expiry Date: Nov 09, 2016
Cancellation Date: Aug 14, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "De Anfang" Rollis Blood Collection Needle (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8334302c78e8c997bd979c7351f51ce5 and manufactured by LERNAPHARM INC.;; STERILANCE MEDICAL (SUZHOU) INC.. The authorized representative in Taiwan is U-E CHECK MEDICAL CO., LTD..

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