Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

J 22132 — Class I MDR by PROTETIKA, a.s.

MD Atlas
PROTETIKA, a.s.

EUDAMED last updated this device on May 14, 2026

J 22132

858500J22132CL3XSXLCE

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PROTETIKA, a.s.
UDI-DI code: 08585003405967
Reference / catalog number: J 22132

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?

View device family (Basic UDI)

Manufacturer information

Organization name: PROTETIKA, a.s.
SRN: SK-MF-000004489
Manufacturer status: Active

Related devices

J 39794858500J39794I3FFOn the market J 39795858500J39795II1FYOn the market J 39797858500J39797II3GJOn the market J 39796858500J39796II2G9On the market J 22160858500J22160IIIMCGOn 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.

Critical warnings

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

CW275
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Slovakia; available across 3 countries total.

Country	On market since	Until
SlovakiaPrimary placement		Still on market
Czechia		Still on market
Latvia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08585003405967
Basic UDI-DI: 858500J22132CL3XSXLCE
Reference / catalog number: J 22132
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: Neoprénová bandáž členka, ČL-3, veľkosť XS/XL
Additional information URL: https://www.protetika.sk/
Clinical sizes: Ankle circumference (cm) 18-34

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Y06120601PASSIVE ANKLE-FOOT ORTHOSES

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

Become a partner of MD Atlas