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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

04B0S040 — Class I MDR by Megapharma Ospedaliera…

MD Atlas
Megapharma Ospedaliera s.r.l.

EUDAMED last updated this device on Apr 30, 2026

04B0S040

80569779804X00BC

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Megapharma Ospedaliera s.r.l.
UDI-DI code: 08056977981318
Reference / catalog number: 04B0S040

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View device family (Basic UDI)

Manufacturer information

Organization name: Megapharma Ospedaliera s.r.l.
SRN: IT-MF-000010739
Manufacturer status: Active

Related devices

04B0S03080569779804X00BCOn the market 04B0S020 80569779804X00BCOn the market 04B0S01080569779804X00BCOn the market 04B0S05080569779804X00BCOn the market 04BD003080569779840BD0A7On 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

3 warnings recorded — scroll inside the panel to see all entries.

CW011
EUDAMED did not publish a description for this code.
CW030
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08056977981318
Basic UDI-DI: 80569779804X00BC
Reference / catalog number: 04B0S040
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: Bendaggio braccio-spalla, immobilizzatore scapolo-omerale.
Additional information URL: https://www.megapharma.it/
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)08056977981318

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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.

M030501IMMOBILISATION BANDAGES FOR SHOULDER, ARM AND COLLARBONE

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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