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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

J 22117 — Class I MDR by PROTETIKA, a.s.

MD Atlas
PROTETIKA, a.s.

EUDAMED last updated this device on Jan 23, 2026

J 22117

858500J22117PA2XXLX5

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PROTETIKA, a.s.
UDI-DI code: 08585003406018
Reference / catalog number: J 22117

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View device family (Basic UDI)

Manufacturer information

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

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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.

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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: 08585003406018
Basic UDI-DI: 858500J22117PA2XXLX5
Reference / catalog number: J 22117
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 drieku, PA-2, veľkosť XXL
Additional information URL: https://www.protetika.sk/
Clinical sizes: Waist circumference 110 - 118 cm; Back height of prostheses 26,5 cm

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.

Y060308LUMBOSACRAL SPINE 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

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