Taiwan FDA registration 4557ecee6704a3ff1a7f7b142a4f3979

Le Ke Mi Catheter Fixation Device (Sterilized)

TW: 樂珂渼導管固定裝置(滅菌)

Taiwan·Risk Class 1·BSN medical GmbH;; BSN MEDICAL GMBH·Registered Jun 04, 2024 – Jun 04, 2029Active

Registration details

Analysis ID: 4557ecee6704a3ff1a7f7b142a4f3979
Customs Code: DHA09402349807

Company information

Manufacturer: BSN medical GmbH;; BSN MEDICAL GMBH
Manufacturer Country: Germany
Authorized Representative: GLORIA BIOMED CO., LTD.

Product details

Intended Use: It is limited to the first level identification scope of the Intravascular Catheter Fixation Device (J.5210) of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5210 血管內導管固定裝置
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jun 04, 2024
Expiry Date: Jun 04, 2029

About this record

Access comprehensive regulatory information for Le Ke Mi Catheter Fixation Device (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4557ecee6704a3ff1a7f7b142a4f3979 and manufactured by BSN medical GmbH;; BSN MEDICAL GMBH. The authorized representative in Taiwan is GLORIA BIOMED CO., LTD..

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