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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

6450 I — Class IIa MDR by Med SSE System GmbH

MD Atlas
Med SSE System GmbH

EUDAMED last updated this device on Apr 7, 2026

6450 I

PP19221VT213

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Med SSE System GmbH
UDI-DI code: 111691529181
Reference / catalog number: 6450 I

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Manufacturer information

Organization name: Med SSE System GmbH
SRN: DE-MF-000008104
Manufacturer status: Active

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7401PP19221ZB485On the market 7400PP19221ZB485On the market 1636PP19221AT107On the market 1628PP19221AT107On the market 1160PP19221AT107On the market

Critical warnings

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

CW275
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 111691529181
Basic UDI-DI: PP19221VT213
Reference / catalog number: 6450 I
Issuing entity: IFA

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: The inner bore makes it easier to insert the tampon using an applicator and position it correctly. This can be particularly beneficial for patients with limited mobility.
Additional information URL: https://www.medsse.de/produkte/contam_vaginaltampons/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

U070199INTERNAL SYSTEMS FOR THE TREATMENT OF INCONTINENCE - 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

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.