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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

20901 — Class I MDR by GIMA SPA

MD Atlas
GIMA SPA

EUDAMED last updated this device on May 29, 2026

20901

80232790000T02070000000NX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: GIMA SPA
UDI-DI code: 08023279209013
Reference / catalog number: 20901

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View device family (Basic UDI)

Manufacturer information

Organization name: GIMA SPA
SRN: IT-MF-000011004
Manufacturer status: Active

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Certificates

Certificate health across this manufacturer's portfolio.

IT349382Issued
Quality assuranceNotified body: 1370Expiry: Jan 26, 2030

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Italy; available across 3 countries total.

Country	On market since	Until
ItalyPrimary placement		Still on market
Spain		Still on market
Luxembourg		Still on market

Device identification

Trade name: not provided
UDI-DI code: 08023279209013
Basic UDI-DI: 80232790000T02070000000NX
Reference / catalog number: 20901
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.

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.

T0207CAPS AND HEADWEAR (EXCLUDING PERSONAL PROTECTIVE EQUIPMENT - PPE)

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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