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

Vlab-Basic — Class IIa MDR by EKOVUK MEDI, s.r.o.

MD Atlas
EKOVUK MEDI, s.r.o.

EUDAMED last updated this device on Apr 3, 2024

Vlab-Basic

859421244VLABLF

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EKOVUK MEDI, s.r.o.
UDI-DI code: 08594212440133
Reference / catalog number: Vlab-Basic

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: EKOVUK MEDI, s.r.o.
SRN: CZ-MF-000040403
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Czechia; available across 2 countries total.

Country	On market since	Until
CzechiaPrimary placement	Jan 1, 2010	Still on market
Slovakia	Jan 1, 2010	Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594212440133
Basic UDI-DI: 859421244VLABLF
Reference / catalog number: Vlab-Basic
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Plethysmographic device for complete non-invasive vascular diagnostics
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

C0180ARTERO-VENOUS SYSTEM DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES

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

Related devices

BIOM 7.8859421244BIOMHLOn the market Leg sleeve with 14 chambers859421244PNEUVEN27On the market Leg sleeve with 7 chambers859421244PNEUVEN27On the market N7R859421244PNEUVEN27On the market N7RR859421244PNEUVEN27On 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.