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Organization name
UDI-DI code
Reference / catalog number

moduversa HF — Class IIb MDR by modul technik GmbH

MD Atlas
modul technik GmbH

EUDAMED last updated this device on Jun 25, 2025

moduversa HF

426241958DVEbe9HJ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: modul technik GmbH
UDI-DI code: 04262419580054
Reference / catalog number: moduversa HF

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Manufacturer information

Organization name: modul technik GmbH
SRN: DE-MF-000014647
Manufacturer status: Active

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 1, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262419580054
Basic UDI-DI: 426241958DVEbe9HJ
Reference / catalog number: moduversa HF
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z120309MEDICAL/MEDICINAL GAS PIPELINE SYSTEMS AND RELATED ACCESSORIES

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

Certificate health across this manufacturer's portfolio.

44911222228Issued
Quality management systemNotified body: 0044Expiry: Dec 2, 2030