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

GM-K4 NYITOTT XL — Class I MDR by PATELLA-96 Kereskedelmi…

MD Atlas
PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság

EUDAMED last updated this device on Apr 12, 2022

GM-K4 NYITOTT XL

599954297GM0939QZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
UDI-DI code: 05999542978234
Reference / catalog number: GM-K4 NYITOTT XL

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: PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság
SRN: HU-MF-000004588
Manufacturer status: Active

Market distribution

Primary placement in Hungary; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 05999542978234
Basic UDI-DI: 599954297GM0939QZ
Reference / catalog number: GM-K4 NYITOTT XL
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)

Y061209KNEE 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

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

GM felnőtt nadrágpelenka S (1200 ml)599954297GM0930QFOn the market ANTIDECUBITUS MATRAC GM BÉZS599954297GM0955QXOn the market ANTIDECUBITUS MATRAC GM KÉK599954297GM0955QXOn the market BOKARÖGZÍTŐ GM LÉGPÁRNÁS BAL599954297GM0938QXOn the market BOKARÖGZÍTŐ GM LÉGPÁRNÁS JOBB599954297GM0938QXOn the market