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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

20930 — Class I MDR by Venner Medical…

MD Atlas
Venner Medical (Deutschland) GmbH

EUDAMED last updated this device on May 29, 2026

20930

426053749PPCH02AR

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Venner Medical (Deutschland) GmbH
UDI-DI code: 04260537490453
Reference / catalog number: 20930

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View device family (Basic UDI)

Manufacturer information

Organization name: Venner Medical (Deutschland) GmbH
SRN: DE-MF-000005934
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 9, 2007	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260537490453
Basic UDI-DI: 426053749PPCH02AR
Reference / catalog number: 20930
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: The PEGA®POUCH 3 is a finished product specifically designed to securely hold the PEGA® PCA, PEGA® plus, and PEGA® light C infu-sion pump and medication bag with PEGA® Disposable in place when utilized by patients.
Additional information URL: https://www.vennermedical.de/
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04260537490453

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

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

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Certificates

Certificate health across this manufacturer's portfolio.

G10 067727 0011Issued
Quality management systemNotified body: 0123Expiry: Jul 17, 2029