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

EZS-10/R — Class I MDR by EGO Zlín, spol. s r.o.

MD Atlas
EGO Zlín, spol. s r.o.

EUDAMED last updated this device on Apr 21, 2026

EZS-10/R

859420647F08EZSA7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EGO Zlín, spol. s r.o.
UDI-DI code: 08594206470214
Reference / catalog number: EZS-10/R

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: EGO Zlín, spol. s r.o.
SRN: CZ-MF-000031911
Manufacturer status: Active

Related devices

AME-FP859420647F09EAM7POn the market EBX859420647F02EBX6XOn the market EBXT859420647F02EBX6XOn the market EZS-10859420647F08EZSA7On the market EBV 30/40 IN-CH859420647F01EBV6LOn 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 1 country total.

Country	On market since	Until
CzechiaPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08594206470214
Basic UDI-DI: 859420647F08EZSA7
Reference / catalog number: EZS-10/R
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: Dětský zádržný systém umožňuje bezpečné upnutí pacienta a následný přenos či převoz na sanitních nosítkách.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08050199PATIENT TRANSFER STRETCHERS - OTHER

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