Taiwan FDA registration a3cd1b59d962c35cd5152f9ee2136987
"Brown" Spitzer Fluid Sleeve
TW: ”柏朗”史倍司輸液套
Taiwan·Risk Class 2·B. Braun Viet Nam Co., Ltd.; B. BRAUN MELSUNGEN AG·Registered Mar 08, 2022 – Mar 08, 2027ActiveRegistration details
- Analysis ID
- a3cd1b59d962c35cd5152f9ee2136987
- Customs Code
- DHA05603531903
Company information
- Manufacturer Country
- Viet Nam;;Germany
- Authorized Representative
- B. BRAUN TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed in the approved Chinese manual. The indication is changed to: detailed as the approved Chinese instruction manual (the original label, instruction manual or packaging approved on March 25, 111 will be withdrawn and invalidated).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
- Mar 08, 2022
- Expiry Date
- Mar 08, 2027
About this record
Access comprehensive regulatory information for "Brown" Spitzer Fluid Sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a3cd1b59d962c35cd5152f9ee2136987 and manufactured by B. Braun Viet Nam Co., Ltd.; B. BRAUN MELSUNGEN AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..
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