AAG120002

Organization name

Medset Medizintechnik GmbH

SRN

DE-MF-000016442

Manufacturer status

Active

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• CW010

  N/A

Primary placement in Germany; available across 3 countries total.

Trade name

not provided

UDI-DI code

04250403709000

Basic UDI-DI

B-04250403709000

Reference / catalog number

AAG120002

Issuing entity

GS1

Risk category

Class IIa

Applicable legislation

MDD [Directive 93/42/EEC on medical devices]

Status

On the market

Quantity

1

Additional product description

The appropriate use of SCANLIGHT III recorder is 24-hour-blood pressure monitoring and pulse wave analysis (PWA). The SCANLIGHT III recorder should be used only under medical supervision. Because of the risk of strangulation from the tube and cuff, the SCANLIGHT III recorder may not be used for patients who are legally incompetent, and must not get into the hands of unsupervised children. The SCANLIGHT III is not designed for the application in neonates and children under the age of 3. The SCANLIGHT III recorder may not be used for blood pressure monitoring in intensive care or during operation.

Additional information URL

No additional information URL provided by the manufacturer.

Clinical sizes

No clinical sizes registered for this device.

• Z1203020501NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGES

• Batch number
• Expiration date
• Manufacturing date
• Serial number
• Software identification