Taiwan FDA registration 1d64a6c5cd830405c0b695e261536b0e

"Schbil" Xinda blood collection needle

TW: “施必爾”信達採血針

Taiwan·Risk Class 1·SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.·Registered Apr 27, 2007 – Apr 27, 2012Cancelled

Registration details

Analysis ID: 1d64a6c5cd830405c0b695e261536b0e
Customs Code: DHA04600036701

Company information

Manufacturer: SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.
Manufacturer Country: China
Authorized Representative: Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch

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: Apr 27, 2007
Expiry Date: Apr 27, 2012
Cancellation Date: Sep 26, 2016

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Schbil" Xinda blood collection needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1d64a6c5cd830405c0b695e261536b0e and manufactured by SUZHOU SPR MEDICAL DEVICES DEVELOPMENT CO., LTD.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.

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