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

05999571440757 — Class I MDR by Sala-Med Ortopédtechnika…

MD Atlas
Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.

EUDAMED last updated this device on Apr 22, 2026

05999571440757

5999571440007GH

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.
UDI-DI code: 05999571440757
Reference / catalog number: 05999571440757

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: Sala-Med Ortopédtechnikai és Gyógyászati Segédeszköz Centrum Kft.
SRN: HU-MF-000004191
Manufacturer status: Active

Market distribution

Primary placement in Hungary; available across 1 country total.

Country	On market since	Until
HungaryPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05999571440757
Basic UDI-DI: 5999571440007GH
Reference / catalog number: 05999571440757
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Y060399SPINE ORTHOSES - 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

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.

Related devices

059995714409175999571440010G6On the market 059995714409245999571440010G6On the market 059995714409315999571440010G6On the market 059995714409485999571440010G6On the market 059995714416485999571440016GJOn the market