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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

800 PLUS 2887789 — Class I MDR by BRENTAFLEX SRL SOCIETÀ…

MD Atlas
BRENTAFLEX SRL SOCIETÀ BENEFIT

EUDAMED last updated this device on Nov 3, 2025

800 PLUS 2887789

805233441MTR0026G

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BRENTAFLEX SRL SOCIETÀ BENEFIT
UDI-DI code: 08052334410859
Reference / catalog number: 800 PLUS 2887789

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View device family (Basic UDI)

Manufacturer information

Organization name: BRENTAFLEX SRL SOCIETÀ BENEFIT
SRN: IT-MF-000029029
Manufacturer status: Active

Related devices

1500 MEMO PLUS 2887788805233441MTR0026GOn the market 1500 MEMO PLUS 2887788805233441MTR0026GOn the market 1500 MEMO PLUS 2887788805233441MTR0026GOn the market 800 2887790805233441MTR0026GOn the market 800 2887790805233441MTR0026GOn 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

No critical warnings reported for this device.

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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: 08052334410859
Basic UDI-DI: 805233441MTR0026G
Reference / catalog number: 800 PLUS 2887789
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: Double Pocketed Spring & Foam / Memory Foam Mattresses
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)08052334410859

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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.

V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSES

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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