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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

P302C51501HW — Class I MDR by SYSTEM ASSISTANCE MEDICAL

MD Atlas
SYSTEM ASSISTANCE MEDICAL

EUDAMED last updated this device on Dec 11, 2025

P302C51501HW

37003686P302CHW1ZB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SYSTEM ASSISTANCE MEDICAL
UDI-DI code: 03700368612682
Reference / catalog number: P302C51501HW

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Manufacturer information

Organization name: SYSTEM ASSISTANCE MEDICAL
SRN: FR-MF-000003517
Manufacturer status: Active

Related devices

SYST'AM P111MPPMHI37003686P111MHI1Z7On the market P301C40431HW37003686P301CHW1YYOn the market P301C43431HW37003686P301CHW1YYOn the market P301C46461HW37003686P301CHW1YYOn the market P302C43431HW37003686P302CHW1ZBOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: 03700368612682
Basic UDI-DI: 37003686P302CHW1ZB
Reference / catalog number: P302C51501HW
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: SYST'AM P302C-POLYAIR100 CUSHION, 51x50 xm/20''x20'', WITH POLYMAILLE COVER
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V08030102NON-ACTIVE ANTI-DECUBITUS MEDICAL CUSHIONS

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.