Taiwan FDA registration ea362820e026cf8f2b5afdeb49a27fde

"Remeng" Vickiella Neisseria meningococcus A, C, Y, W135 detection kit

TW: "銳盟" 威克菌奈瑟氏腦膜炎球菌A,C,Y,W135群檢測套組

Taiwan·Risk Class 2·REMEL EUROPE LIMITED·Registered Jan 26, 2006 – Jan 26, 2016Cancelled

Registration details

Analysis ID: ea362820e026cf8f2b5afdeb49a27fde
Customs Code: DHA00601594905

Company information

Manufacturer: REMEL EUROPE LIMITED
Manufacturer Country: United Kingdom
Authorized Representative: SCN TRADING COMPANY LIMITED

Product details

Intended Use: 快速乳膠檢測法定性偵測體液或在血液培養中的奈瑟氏腦膜炎(腦膜炎球菌)A,C,Y,W135群的抗原.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3390 奈瑟氏菌屬直接血清試劑
Import Information: import

Dates and status

Registration Date: Jan 26, 2006
Expiry Date: Jan 26, 2016
Cancellation Date: Jan 17, 2017

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Remeng" Vickiella Neisseria meningococcus A, C, Y, W135 detection kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ea362820e026cf8f2b5afdeb49a27fde and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is SCN TRADING COMPANY LIMITED.

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