Taiwan FDA registration 555fb46446d791bdb4e321d1b04d8b1e

"Siemens" gram-negative bacteria synergistic vertex composite test group seven

TW: “西門子”革蘭氏陰性菌協同折點複合檢驗組七型

Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered Jun 12, 2012 – Jun 12, 2017Cancelled

Registration details

Analysis ID: 555fb46446d791bdb4e321d1b04d8b1e
Customs Code: DHA00602365102

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States
Authorized Representative: SIEMENS LIMITED

Product details

Intended Use: Qualitative and/or quantitative determination of resistance to fast-growing aerobic and facultative anaerobic gram-negative bacilli and/or identification of their species.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.1645 Automatic Antibiotic Sensitivity Test System for Short Incubation Period
Import Information: import

Dates and status

Registration Date: Jun 12, 2012
Expiry Date: Jun 12, 2017
Cancellation Date: Dec 13, 2019

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Siemens" gram-negative bacteria synergistic vertex composite test group seven in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 555fb46446d791bdb4e321d1b04d8b1e and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is SIEMENS LIMITED.

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