Taiwan FDA registration d1f65db1b258b347f754f1f1a6ea1c1f

Renault "Siemens" disposable inoculator - group D (unsterilized)

TW: "西門子"雷諾可拋棄式接種器-D組(未滅菌)

Taiwan·Risk Class 1·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Registered May 19, 2008 – May 19, 2018Cancelled

Registration details

Analysis ID: d1f65db1b258b347f754f1f1a6ea1c1f
Customs Code: DHA04400675103

Company information

Manufacturer: SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Country: United States
Authorized Representative: BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)

Product details

Intended Use: Limited to the first level identification range of microtitration dilution and dispensing equipment (C.2500) of the management measures for medical devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2500 微滴定稀釋及分配器材
Import Information: import

Dates and status

Registration Date: May 19, 2008
Expiry Date: May 19, 2018
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 Renault "Siemens" disposable inoculator - group D (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d1f65db1b258b347f754f1f1a6ea1c1f and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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