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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

KIT 002 — Class I MDR by Excellent Systems A/S

MD Atlas
Excellent Systems A/S

EUDAMED last updated this device on May 27, 2026

KIT 002

5708066DK25276183MDRHT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Excellent Systems A/S
UDI-DI code: 05708066001713
Reference / catalog number: KIT 002

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View device family (Basic UDI)

Manufacturer information

Organization name: Excellent Systems A/S
SRN: DK-MF-000014754
Manufacturer status: Active

Related devices

KIT 0015708066DK25276183MDRHTOn the market KIT 001 N5708066DK25276183MDRHTOn the market KIT 001 S5708066DK25276183MDRHTOn the market KIT 002 N5708066DK25276183MDRHTOn the market KIT 002 N P5708066DK25276183MDRHTOn 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

No critical warnings reported for this device.

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Market distribution

Primary placement in Denmark; available across 1 country total.

Country	On market since	Until
DenmarkPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05708066001713
Basic UDI-DI: 5708066DK25276183MDRHT
Reference / catalog number: KIT 002
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: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

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

Y183015PORTABLE RAMPS

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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