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

5300 VD-04 — Class I MDR by RAMED Kopřivnice s.r.o.

MD Atlas
RAMED Kopřivnice s.r.o.

EUDAMED last updated this device on Apr 15, 2026

5300 VD-04

859420869SOSVDVQ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RAMED Kopřivnice s.r.o.
UDI-DI code: 08594208690603
Reference / catalog number: 5300 VD-04

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: RAMED Kopřivnice s.r.o.
SRN: CZ-MF-000043587
Manufacturer status: Active

Related devices

2520-04859420869ERSPDQZOn the market 2520-06859420869ERSPDQZOn the market 2420-02859420869ERSPDQZOn the market 2520-07859420869ERSPDQZOn the market 2520-02859420869ERSPDQZOn 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.

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement	Oct 27, 2017	Dec 31, 9999
Slovakia		Dec 31, 9999

Device identification

Trade name: not provided
UDI-DI code: 08594208690603
Basic UDI-DI: 859420869SOSVDVQ
Reference / catalog number: 5300 VD-04
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)

Z12011202OPERATING TABLES

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