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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

ATMOS S 351 NATAL mobile with… — Class IIa MDD

MD Atlas
ATMOS MedizinTechnik GmbH & Co. KG

EUDAMED last updated this device on Sep 8, 2025

ATMOS S 351 NATAL mobile with foot control, 230 V

B-04250365139853

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: ATMOS MedizinTechnik GmbH & Co. KG
UDI-DI code: 04250365139853
Reference / catalog number: 444.0482.0

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Manufacturer information

Organization name: ATMOS MedizinTechnik GmbH & Co. KG
SRN: DE-MF-000005570
Manufacturer status: Active

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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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW999
Medical contra-indications: Not adapted: for the continuous operation in case of drainages in the low vacuum range (e.g. thoracic drainage or wound drainage), for smoke evacuation, for liposuction, for the case of emergency or rescue operation Other contra-indications: No application outside of the medical sector. No suction of flammable, corrosive and explosive substances

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: ATMOS S 351 NATAL mobile with foot control, 230 V
UDI-DI code: 04250365139853
Basic UDI-DI: B-04250365139853
Reference / catalog number: 444.0482.0
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12080301OBSTETRIC VACUUM EXTRACTORS

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

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