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Organization name
UDI-DI code
Reference / catalog number

UNT-CD3840.40 — Class I MDR by Unintech GmbH

MD Atlas
Unintech GmbH

EUDAMED last updated this device on May 5, 2026

UNT-CD3840.40

426070601031CHHP

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Unintech GmbH
UDI-DI code: 04260706010062
Reference / catalog number: UNT-CD3840.40

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Manufacturer information

Organization name: Unintech GmbH
SRN: DE-MF-000005136
Manufacturer status: Active

Related devices

UNT-CD2560.20426070601031CHHPOn the market UNT-CD1080.10426070601031CHHPOn the market UNT-LC3000426070601031LGJGOn the market UNT-LC3000.35426070601031LGJGOn the market UNT-LC2300426070601031LGJGOn 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.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
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: 04260706010062
Basic UDI-DI: 426070601031CHHP
Reference / catalog number: UNT-CD3840.40
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: No additional information URL provided by the manufacturer.
Clinical sizes: 45 MU50
46.5 MU50
149 MU50

EMDN nomenclature code(s)

Z12020401INTEGRATED SYSTEMS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES

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