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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 003 P — Class I MDR by Excellent Systems A/S

MD Atlas
Excellent Systems A/S

EUDAMED last updated this device on May 29, 2026

KIT 003 P

5708066DK25276183MDRHT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Excellent Systems A/S
UDI-DI code: 05708066002048
Reference / catalog number: KIT 003 P

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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 0025708066DK25276183MDRHTOn the market KIT 002 N5708066DK25276183MDRHTOn 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: 05708066002048
Basic UDI-DI: 5708066DK25276183MDRHT
Reference / catalog number: KIT 003 P
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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