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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

CR5-A027-012 — Class I MDR by S.A.R.L. PROCOMEDIC

MD Atlas
S.A.R.L. PROCOMEDIC

EUDAMED last updated this device on May 10, 2023

CR5-A027-012

3664595COUSSINC7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: S.A.R.L. PROCOMEDIC
UDI-DI code: 03664595000318
Reference / catalog number: CR5-A027-012

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Manufacturer information

Organization name: S.A.R.L. PROCOMEDIC
SRN: FR-MF-000034841
Manufacturer status: Active

Related devices

DC18-A027-0123664595COUSSINC7On the market T601808-A027-0123664595COUSSINC7On the market T602004-A027-0123664595COUSSINC7On the market T1202008-A027-0123664595COUSSINC7On the market T1002008-A027-0123664595COUSSINC7On 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.

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: 03664595000318
Basic UDI-DI: 3664595COUSSINC7
Reference / catalog number: CR5-A027-012
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: Coussin rectangulaire hauteur 5 cm
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER

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