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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

1091107 — Class I MDR by Akzenta International SA

MD Atlas
Akzenta International SA

EUDAMED last updated this device on Apr 28, 2026

1091107

42504766STAB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Akzenta International SA
UDI-DI code: 04250476612665
Reference / catalog number: 1091107

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Manufacturer information

Organization name: Akzenta International SA
SRN: CH-MF-000036434
Manufacturer status: Active

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GLODL29-AKZ-WH-S0142504766GLOUPOn the market GLODL29-AKZ-WH-M0142504766GLOUPOn the market GLODL29-AKZ-WH-LL142504766GLOUPOn the market GLODL29-AKZ-WH-XS142504766GLOUPOn the market GLODL53-AKZ-WH-S0142504766GLOUPOn the market

Market distribution

Primary placement in Italy; available across 1 country total.

Country	On market since	Until
ItalyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250476612665
Basic UDI-DI: 42504766STAB
Reference / catalog number: 1091107
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: 4
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 200 MU36
100 MU50

EMDN nomenclature code(s)

S01020101FLAT STERILISATION REELS, PAPER/PLASTIC FILM

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.