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Organization name
UDI-DI code
Reference / catalog number

UNT-XI-542695K-HWS — Class I MDR by Unintech GmbH

MD Atlas
Unintech GmbH

EUDAMED last updated this device on May 21, 2026

UNT-XI-542695K-HWS

426070601111containerUT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Unintech GmbH
UDI-DI code: 04262478190737
Reference / catalog number: UNT-XI-542695K-HWS

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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-CD3840.40426070601031CHHPOn the market UNT-CD1080.10426070601031CHHPOn the market UNT-LC3000426070601031LGJGOn the market UNT-LC3000.35426070601031LGJGOn 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: 04262478190737
Basic UDI-DI: 426070601111containerUT
Reference / catalog number: UNT-XI-542695K-HWS
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: 116 MU50
233 MU50
506 MU50

EMDN nomenclature code(s)

S010401TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS

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
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Software identification