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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

V100200 — Class I MDR by E.E.H. ug (Haftungsbesch…

MD Atlas
E.E.H. ug (Haftungsbeschränkt)

EUDAMED last updated this device on Dec 31, 2025

V100200

6580989V90200SR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: E.E.H. ug (Haftungsbeschränkt)
UDI-DI code: 08720892016621
Reference / catalog number: V100200

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Manufacturer information

Organization name: E.E.H. ug (Haftungsbeschränkt)
SRN: DE-MF-000045659
Manufacturer status: Active

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: 08720892016621
Basic UDI-DI: 6580989V90200SR
Reference / catalog number: V100200
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: —
Additional information URL: https://www.evatex.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - 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

V802006580989V90200SROn the market V901906580989V90200SROn the market V1202006580989V90200SROn the market V902006580989V90200SROn the market

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.