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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

106522.020.07 — Class I MDR by Brilliant Group BV

MD Atlas
Brilliant Group BV

EUDAMED last updated this device on May 12, 2026

106522.020.07

8720589175106522PM

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Brilliant Group BV
UDI-DI code: 08720589175310
Reference / catalog number: 106522.020.07

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View device family (Basic UDI)

Manufacturer information

Organization name: Brilliant Group BV
SRN: NL-MF-000050404
Manufacturer status: Active

Related devices

106522.030.0787202993649106522REOn the market 106522.030.1087202993649106522REOn the market 106522.030.0987202993649106522REOn the market 106522.030.0887202993649106522REOn the market 124368.030.09872096417124368QBOn 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.

CW022
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement	May 12, 2026	Dec 31, 2099

Device identification

Trade name: not provided
UDI-DI code: 08720589175310
Basic UDI-DI: 8720589175106522PM
Reference / catalog number: 106522.020.07
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: 100
Additional product description: -
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)08720589175310

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

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

T01020204NITRILE EXAMINATION / TREATMENT GLOVES

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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