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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

2103 - 011 — Class I MDR by Univent Medical GmbH

MD Atlas
Univent Medical GmbH

EUDAMED last updated this device on Mar 23, 2026

2103 - 011

426068838200125

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Univent Medical GmbH
UDI-DI code: 04260688381112
Reference / catalog number: 2103 - 011

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Manufacturer information

Organization name: Univent Medical GmbH
SRN: DE-MF-000015594
Manufacturer status: Active

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4002 - 006426068838400X4XOn the market 4003 - 006426068838400X4XOn the market 4004 - 006426068838400X4XOn the market 2102 - 011426068838200125On the market 2103426068838200125On the market

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 04260688381112
Basic UDI-DI: 426068838200125
Reference / catalog number: 2103 - 011
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: 1
Additional product description: Dual-use Atemschutzmaske - Medizinische Gesichtsmaske TypIIR und FFP2 Maske
Additional information URL: https://www.univent-medical.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T020604MEDICAL USE FACE MASKS, TYPE II AND IIR

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.