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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

011-01402 — Class IIa MDD by Sensatronic GmbH

MD Atlas
Sensatronic GmbH

EUDAMED last updated this device on Oct 28, 2025

011-01402

B-04260651380418

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Sensatronic GmbH
UDI-DI code: 04260651380418
Reference / catalog number: 011-01402

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Manufacturer information

Organization name: Sensatronic GmbH
SRN: DE-MF-000004927
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Oct 28, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260651380418
Basic UDI-DI: B-04260651380418
Reference / catalog number: 011-01402
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: 9 MU170

EMDN nomenclature code(s)

V03010299BODY TEMPERATURE MONITORING PROBES - OTHER

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.