Taiwan FDA registration d720b37433de3b318cdf362552043d36

"Birlanc" Combert infusion sleeve

TW: “柏朗” 康貝特輸液套

Taiwan·Risk Class 2·B. Braun Medical Kft Production Division;; B. BRAUN MELSUNGEN AG·Registered May 11, 2023 – May 11, 2028Active

Registration details

Analysis ID: d720b37433de3b318cdf362552043d36
Customs Code: DHA05603636005

Company information

Manufacturer: B. Braun Medical Kft Production Division;; B. BRAUN MELSUNGEN AG
Manufacturer Country: Hungary;;Germany
Authorized Representative: B. BRAUN TAIWAN CO., LTD.

Product details

Intended Use: Details as approved Chinese instructions Change of efficacy, use or indications: Details as approved Chinese instructions (the original label, instructions or packaging approved on June 8, 112 will be withdrawn and invalidated).
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5440 血管內輸液套
Import Information: import

Dates and status

Registration Date: May 11, 2023
Expiry Date: May 11, 2028

About this record

Access comprehensive regulatory information for "Birlanc" Combert infusion sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d720b37433de3b318cdf362552043d36 and manufactured by B. Braun Medical Kft Production Division;; B. BRAUN MELSUNGEN AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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