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

ES-16 — Class I MDR by EGO Zlín, spol. s r.o.

MD Atlas
EGO Zlín, spol. s r.o.

EUDAMED last updated this device on Feb 12, 2026

ES-16

859420647F04ESD7Q

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: 08594206470122
Reference / catalog number: ES-16

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-10/R859420647F08EZSA7On the market EZS-10859420647F08EZSA7On 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.

Placed on the market in Czechia; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 08594206470122
Basic UDI-DI: 859420647F04ESD7Q
Reference / catalog number: ES-16
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: Vakuová dlaha je prostředek pro poskytování první pomoci. Zajistí šetrnou fixaci a stabilizaci poraněné dolní končetiny v požadované poloze.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M03050202SYNTHETIC CAST BANDAGES AND SPLINTS

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