Taiwan FDA registration db7b6a3a5760b491279a661839414037

Knooda right heart diagnostic catheter

TW: 克諾達右心診斷導管

Taiwan·Risk Class 2·AESCULAP CHIFA SP. Z O.O.;; B. BRAUN MELSUNGEN AG·Registered Apr 24, 2012 – Apr 24, 2017Cancelled

Registration details

Analysis ID: db7b6a3a5760b491279a661839414037
Customs Code: DHA00602332301

Company information

Manufacturer: AESCULAP CHIFA SP. Z O.O.;; B. BRAUN MELSUNGEN AG
Manufacturer Country: Germany;;Poland
Authorized Representative: B. BRAUN TAIWAN CO., LTD.

Product details

Intended Use: For details, it is Chinese approved copy of the imitation order
Product Type (Level 1): E Cardiovascular Medicine Science
Product Type (Level 2): E.1200 診斷用血管內導管
Import Information: import

Dates and status

Registration Date: Apr 24, 2012
Expiry Date: Apr 24, 2017
Cancellation Date: Nov 20, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Knooda right heart diagnostic catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db7b6a3a5760b491279a661839414037 and manufactured by AESCULAP CHIFA SP. Z O.O.;; B. BRAUN MELSUNGEN AG. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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