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Medical Network News on March 5
Sales in China
First level recall
On March 3, the State Food and Drug Administration announced that Poco International Medical Trading (Shanghai) Co.
, Ltd.
reported that due to the voltage overload in the discharge treatment process involving specific models and specific batches of products, serious defects may be caused.
event.
The manufacturer Boston Scientific Corporation has voluntarily recalled the subcutaneous implantable cardioverter defibrillator (registration number: National Instruments Injection 20153212410).
The recall level is level one.
, Ltd.
reported that due to the voltage overload in the discharge treatment process involving specific models and specific batches of products, serious defects may be caused.
event.
The manufacturer Boston Scientific Corporation has voluntarily recalled the subcutaneous implantable cardioverter defibrillator (registration number: National Instruments Injection 20153212410).
The recall level is level one.
Please refer to the "Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved.
Philips 128 devices recalled
Philips Medical (Suzhou) Co.
, Ltd.
reported that the company found that some of the incisive CT, MX16-slice and Access CT scan beds have problems with the push rod motors installed in the scan bed, which may cause the scan bed to move slowly downwards unexpectedly.
It is now actively recalling , The recall level is two.
, Ltd.
reported that the company found that some of the incisive CT, MX16-slice and Access CT scan beds have problems with the push rod motors installed in the scan bed, which may cause the scan bed to move slowly downwards unexpectedly.
It is now actively recalling , The recall level is two.
Ultrasound diagnostic equipment recall
Yum Co.
ESAOTE SPA pharmnet.
com.
cn/agent_product/" target="_blank">agency person Yum (Shenzhen) Co.
, Ltd.
medical equipment report, due to the magnetic field generator supplier receiving the report, said that the production of components for a particular period of time to achieve the integration of navigation for 3D imaging, virtual In the navigation and virtual puncture functions, there may be insufficient measurement accuracy, which may affect the accuracy of imaging or subcutaneous puncture guidance.
Yum Co.
, Ltd.
ESAOTE SPA voluntarily recalled its ultrasonic diagnostic equipment.
ESAOTE SPA pharmnet.
com.
cn/agent_product/" target="_blank">agency person Yum (Shenzhen) Co.
, Ltd.
medical equipment report, due to the magnetic field generator supplier receiving the report, said that the production of components for a particular period of time to achieve the integration of navigation for 3D imaging, virtual In the navigation and virtual puncture functions, there may be insufficient measurement accuracy, which may affect the accuracy of imaging or subcutaneous puncture guidance.
Yum Co.
, Ltd.
ESAOTE SPA voluntarily recalled its ultrasonic diagnostic equipment.
The recall level is two.
Please refer to the " Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved .
Please refer to the " Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved .
Medical Network News on March 5
Sales in China
First level recall
On March 3, the State Food and Drug Administration announced that Poco International Medical Trading (Shanghai) Co.
, Ltd.
reported that due to the voltage overload in the discharge treatment process involving specific models and specific batches of products, serious defects may be caused.
event.
The manufacturer Boston Scientific Corporation has voluntarily recalled the subcutaneous implantable cardioverter defibrillator (registration number: National Instruments Injection 20153212410).
The recall level is level one.
, Ltd.
reported that due to the voltage overload in the discharge treatment process involving specific models and specific batches of products, serious defects may be caused.
event.
The manufacturer Boston Scientific Corporation has voluntarily recalled the subcutaneous implantable cardioverter defibrillator (registration number: National Instruments Injection 20153212410).
The recall level is level one.
Please refer to the "Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved.
Philips 128 devices recalled
Philips Medical (Suzhou) Co.
, Ltd.
reported that the company found that some of the incisive CT, MX16-slice and Access CT scan beds have problems with the push rod motors installed in the scan bed, which may cause the scan bed to move slowly downwards unexpectedly.
It is now actively recalling , The recall level is two.
, Ltd.
reported that the company found that some of the incisive CT, MX16-slice and Access CT scan beds have problems with the push rod motors installed in the scan bed, which may cause the scan bed to move slowly downwards unexpectedly.
It is now actively recalling , The recall level is two.
Ultrasound diagnostic equipment recall
Yum Co.
ESAOTE SPA pharmnet.
com.
cn/agent_product/" target="_blank">agency person Yum (Shenzhen) Co.
, Ltd.
medical equipment report, due to the magnetic field generator supplier receiving the report, said that the production of components for a particular period of time to achieve the integration of navigation for 3D imaging, virtual In the navigation and virtual puncture functions, there may be insufficient measurement accuracy, which may affect the accuracy of imaging or subcutaneous puncture guidance.
Yum Co.
, Ltd.
ESAOTE SPA voluntarily recalled its ultrasonic diagnostic equipment.
ESAOTE SPA pharmnet.
com.
cn/agent_product/" target="_blank">agency person Yum (Shenzhen) Co.
, Ltd.
medical equipment report, due to the magnetic field generator supplier receiving the report, said that the production of components for a particular period of time to achieve the integration of navigation for 3D imaging, virtual In the navigation and virtual puncture functions, there may be insufficient measurement accuracy, which may affect the accuracy of imaging or subcutaneous puncture guidance.
Yum Co.
, Ltd.
ESAOTE SPA voluntarily recalled its ultrasonic diagnostic equipment.
The recall level is two.
Please refer to the " Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved .
Please refer to the " Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved .
Medical Network News on March 5
Sales in China
First level recall
First level recall On March 3, the State Food and Drug Administration announced that Poco International Medical Trading (Shanghai) Co.
, Ltd.
reported that due to the voltage overload in the discharge treatment process involving specific models and specific batches of products, serious defects may be caused.
event.
The manufacturer Boston Scientific Corporation has voluntarily recalled the subcutaneous implantable cardioverter defibrillator (registration number: National Instruments Injection 20153212410).
The recall level is level one.
, Ltd.
reported that due to the voltage overload in the discharge treatment process involving specific models and specific batches of products, serious defects may be caused.
event.
The manufacturer Boston Scientific Corporation has voluntarily recalled the subcutaneous implantable cardioverter defibrillator (registration number: National Instruments Injection 20153212410).
The recall level is level one.
Please refer to the "Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved.
Philips 128 devices recalled
Philips 128 devices recalled Philips Medical (Suzhou) Co.
, Ltd.
reported that the company found that some of the incisive CT, MX16-slice and Access CT scan beds have problems with the push rod motors installed in the scan bed, which may cause the scan bed to move slowly downwards unexpectedly.
It is now actively recalling , The recall level is two.
Enterprise business enterprise, Ltd.
reported that the company found that some of the incisive CT, MX16-slice and Access CT scan beds have problems with the push rod motors installed in the scan bed, which may cause the scan bed to move slowly downwards unexpectedly.
It is now actively recalling , The recall level is two.
Ultrasound diagnostic equipment recall
Ultrasound diagnostic equipment recall Yum Co.
ESAOTE SPA pharmnet.
com.
cn/agent_product/" target="_blank">agency person Yum (Shenzhen) Co.
, Ltd.
medical equipment report, due to the magnetic field generator supplier receiving the report, said that the production of components for a particular period of time to achieve the integration of navigation for 3D imaging, virtual In the navigation and virtual puncture functions, there may be insufficient measurement accuracy, which may affect the accuracy of imaging or subcutaneous puncture guidance.
Yum Co.
, Ltd.
ESAOTE SPA voluntarily recalled its ultrasonic diagnostic equipment.
pharmnet. ESAOTE SPA pharmnet.
com.
cn/agent_product/" target="_blank">agency person Yum (Shenzhen) Co.
, Ltd.
medical equipment report, due to the magnetic field generator supplier receiving the report, said that the production of components for a particular period of time to achieve the integration of navigation for 3D imaging, virtual In the navigation and virtual puncture functions, there may be insufficient measurement accuracy, which may affect the accuracy of imaging or subcutaneous puncture guidance.
Yum Co.
, Ltd.
ESAOTE SPA voluntarily recalled its ultrasonic diagnostic equipment.
com.
cn/agent_product/" target="_blank">Agentpharmnet.
com.
cn/agent_product/" target="_blank"> Agent Agent
The recall level is two.
Please refer to the " Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved .
Medical equipment medical equipment medical equipmentPlease refer to the " Medical Device Recall Event Report Form" for detailed information such as the model, specification and batch of the product involved .
