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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

171001 — Class IIa MDR by Heyer Medical AG

MD Atlas
Heyer Medical AG

EUDAMED last updated this device on May 20, 2026

171001

4251743800015UU

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Heyer Medical AG
UDI-DI code: 04251743800518
Reference / catalog number: 171001

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Manufacturer information

Organization name: Heyer Medical AG
SRN: DE-MF-000014330
Manufacturer status: Active

Related devices

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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.

CW018
See instruction manual/booklet for warnings and contraindications.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 2, 2026	Mar 1, 2028

Device identification

Trade name: not provided
UDI-DI code: 04251743800518
Basic UDI-DI: 4251743800015UU
Reference / catalog number: 171001
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: No additional information URL provided by the manufacturer.
Clinical sizes: including both adults and children (≥ 3 years old)

EMDN nomenclature code(s)

R060101COLD NEBULISATION SYSTEMS

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