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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

802104 — Class I MDR by Igazgyöngy '98…

MD Atlas
Igazgyöngy '98 Kereskedelmi és Szolgáltató Kft.

EUDAMED last updated this device on Oct 3, 2023

802104

5999862229802KZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Igazgyöngy '98 Kereskedelmi és Szolgáltató Kft.
UDI-DI code: 05999862229276
Reference / catalog number: 802104

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Manufacturer information

Organization name: Igazgyöngy '98 Kereskedelmi és Szolgáltató Kft.
SRN: HU-MF-000021484
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: 05999862229276
Basic UDI-DI: 5999862229802KZ
Reference / catalog number: 802104
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: 11.7–12.3 MU10
360–440 MU10

EMDN nomenclature code(s)

M0304010203ELASTIC COMPRESSION BANDAGES, COHESIVE, HIGH EXTENSIBILITY (>140%)

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

Related devices

This device is not currently linked to any other device.

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.