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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

AAG127102 — Class IIa MDR by Medset Medizintechnik…

MD Atlas
Medset Medizintechnik GmbH

EUDAMED last updated this device on Dec 17, 2024

AAG127102

42504037AAG127000-00BY

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Medset Medizintechnik GmbH
UDI-DI code: 04250403720197
Reference / catalog number: AAG127102

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Manufacturer information

Organization name: Medset Medizintechnik GmbH
SRN: DE-MF-000016442
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement	Dec 3, 2024	Still on market
Czechia	Dec 3, 2024	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250403720197
Basic UDI-DI: 42504037AAG127000-00BY
Reference / catalog number: AAG127102
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://medset.zendesk.com/hc/de/articles/360021587159-Gebrauchsanweisungen-Instruction-for-use
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12030292VITAL SIGNS MONITORING INSTRUMENTS - MEDICAL DEVICE SOFTWARE

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.