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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

MamaSafe 20 pairs — Class I MDR by MSP Medizintechnik GmbH

MD Atlas
MSP Medizintechnik GmbH

EUDAMED last updated this device on Aug 9, 2022

MamaSafe 20 pairs

912004788HSOMASANE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: MSP Medizintechnik GmbH
UDI-DI code: 09120047882757
Reference / catalog number: HSOMASA20

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Manufacturer information

Organization name: MSP Medizintechnik GmbH
SRN: AT-MF-000018341
Manufacturer status: Inactive

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

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: MamaSafe 20 pairs
UDI-DI code: 09120047882757
Basic UDI-DI: 912004788HSOMASANE
Reference / catalog number: HSOMASA20
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: 20
Additional product description: Die MamaSafe Brustwarzenschutzringe unterstützen den Heilungsprozess von wunden Brustwarzen – die durch das Stillen verursacht werden. MamaSafe schützt die Brustwarzen vor dem Verkleben mit der Kleidung und lässt die Luft ungehindert zirkulieren.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M040499DRESSINGS FOR WOUNDS, SORES AND ULCERATIONS - 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

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.