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

0032133-005-035 — Class I MDR by DZO s.r.o.

MD Atlas
DZO s.r.o.

EUDAMED last updated this device on Sep 24, 2025

0032133-005-035

859405200444G7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: DZO s.r.o.
UDI-DI code: 08594052008951
Reference / catalog number: 0032133-005-035

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: DZO s.r.o.
SRN: CZ-MF-000037146
Manufacturer status: Active

Related devices

0032125-001-009859405200333FVOn the market 0032117-002-070859405200111F9On the market 0032117-002-068859405200111F9On the market 0032117-002-064859405200111F9On the market 0032117-002-060859405200111F9On 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: 08594052008951
Basic UDI-DI: 859405200444G7
Reference / catalog number: 0032133-005-035
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: 020T modrá - reflex
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: modrá, reflex+tm.podešev
EU 38

EMDN nomenclature code(s)

Y063303READY-MADE ORTHOTIC SHOES

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