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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

LIBERIS — Class I MDR by CARPENTER ENGINEERED…

MD Atlas
CARPENTER ENGINEERED FOAMS SAS

EUDAMED last updated this device on May 12, 2025

LIBERIS

3011570000105423747M1L6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CARPENTER ENGINEERED FOAMS SAS
UDI-DI code: 03157000000008
Reference / catalog number: LIBERIS

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Manufacturer information

Organization name: CARPENTER ENGINEERED FOAMS SAS
SRN: FR-MF-000044494
Manufacturer status: Active

Critical warnings

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

CW999
Ne convient pas aux patients présentant une anatomie atypique
CW999
N‘est pas conçu pour entrer en contact direct avec la peau lésée
CW999
Destiné à être utilisé sur des lits médicalisés

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: LIBERIS
UDI-DI code: 03157000000008
Basic UDI-DI: 3011570000105423747M1L6
Reference / catalog number: LIBERIS
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.

EMDN nomenclature code(s)

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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

MOBILIS3011570000106624547M1MSOn the market VITALIS3011570000108482547M1QEOn 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.