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Organization name
UDI-DI code
Reference / catalog number

Carebag ® Protège seau, boîte de 20 — Class I MDR by CLEANIS

MD Atlas
CLEANIS

EUDAMED last updated this device on Aug 27, 2025

Carebag ® Protège seau, boîte de 20

376005923RECUEILEXCDT01AY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CLEANIS
UDI-DI code: 03760059230069
Reference / catalog number: 7831738

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Manufacturer information

Organization name: CLEANIS
SRN: FR-MF-000004677
Manufacturer status: Active

Critical warnings

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

CW999
En cas de réutilisation risque d’absorption insuffisante voire nulle e donc de contamination potentielle et d’inconfort pour le patient, En cas de contact du tampon avec l’œil ou les muqueuses, rincer abondamment à l’eau. En cas de gêne persistante, contacter votre médecin. Ne pas mettre en contact de peau lésée. Ne pas laisser à la portée des enfants. En cas d’ingestion, consulter immédiatement un médecin et lui montrer l’emballage.

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: Carebag ® Protège seau, boîte de 20
UDI-DI code: 03760059230069
Basic UDI-DI: 376005923RECUEILEXCDT01AY
Reference / catalog number: 7831738
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: 20
Additional product description: Protège seau de chaise percée à liens coulissants muni d'un tampon super-absorbant (capacité d’absorption de 450ml saline 0,9%, équivalence fluides biologiques),destiné au recueil des excreta.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V0880MEDICAL SUPPORT EQUIPMENT - ACCESSORIES

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

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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.