Taiwan FDA registration 90c6309cf010e0f4f1b02475cedcd407

"Bidi" active blood collection needle

TW: "必帝" 主動式採血針

Taiwan·Risk Class 1·HTL - STREFA SP. Z.O.O.·Registered Mar 29, 2007 – Mar 29, 2012Cancelled

Registration details

Analysis ID: 90c6309cf010e0f4f1b02475cedcd407
Customs Code: DHA04400571800

Company information

Manufacturer: HTL - STREFA SP. Z.O.O.
Manufacturer Country: Poland
Authorized Representative: Taiwan Branch of American Business Bidi 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: import

Dates and status

Registration Date: Mar 29, 2007
Expiry Date: Mar 29, 2012
Cancellation Date: Apr 14, 2014

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Bidi" active 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 90c6309cf010e0f4f1b02475cedcd407 and manufactured by HTL - STREFA SP. Z.O.O.. The authorized representative in Taiwan is Taiwan Branch of American Business Bidi Co., Ltd.

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