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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

550201 — Class I MDR by IVF HARTMANN AG

MD Atlas
IVF HARTMANN AG

EUDAMED last updated this device on Mar 23, 2026

550201

76116003296N5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: IVF HARTMANN AG
UDI-DI code: 07611600953424
Reference / catalog number: 550201

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Manufacturer information

Organization name: IVF HARTMANN AG
SRN: CH-MF-000015962
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.

Market distribution

Primary placement in Austria; available across 1 country total.

Placed on the market in Austria; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 07611600953424
Basic UDI-DI: 76116003296N5
Reference / catalog number: 550201
Issuing entity: GS1

Classification

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

Device details

Quantity: 10
Additional product description: Dressing
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 7.5 MU10
5 MU10

EMDN nomenclature code(s)

M040204NON-ADHERENT ABSORBENT DRESSINGS

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
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Software identification