Taiwan FDA registration d4e0cd255522f8cda72739925e322b4e

"Subir" blood lancet

TW: "蘇必爾" 採血針

Taiwan·Risk Class 1·SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Jun 02, 2006 – Jun 02, 2011Cancelled

Registration details

Analysis ID: d4e0cd255522f8cda72739925e322b4e
Customs Code: DHA04600025901

Company information

Manufacturer: SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.
Manufacturer Country: China
Authorized Representative: ECHEAL 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: Input;; Chinese goods

Dates and status

Registration Date: Jun 02, 2006
Expiry Date: Jun 02, 2011
Cancellation Date: Nov 20, 2012

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Subir" blood lancet in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d4e0cd255522f8cda72739925e322b4e and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is ECHEAL CO., LTD..

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