Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

Quickramp 006G — Class I MDR by Excellent Systems A/S

MD Atlas
Excellent Systems A/S

EUDAMED last updated this device on May 21, 2026

Quickramp 006G

5708066DK25276183MDRHT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Excellent Systems A/S
UDI-DI code: 05708066000570
Reference / catalog number: Quickramp 006G

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Related devices

Quickramp 004A5708066DK25276183MDRHTOn the market Quickramp 004C5708066DK25276183MDRHTOn the market Quickramp 004E5708066DK25276183MDRHTOn the market Quickramp 004G5708066DK25276183MDRHTOn the market Quickramp 006A5708066DK25276183MDRHTOn the market

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: 05708066000570
Basic UDI-DI: 5708066DK25276183MDRHT
Reference / catalog number: Quickramp 006G
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.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.