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Organization name
UDI-DI code
Reference / catalog number

Carebag sac vomitoire avec sachet… — Class I MDR by CLEANIS

MD Atlas
CLEANIS

EUDAMED last updated this device on Aug 27, 2025

Carebag sac vomitoire avec sachet PRO, boîte de 20

376005923RECUEILEXCDT01AY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CLEANIS
UDI-DI code: 03760059239208
Reference / catalog number: 7733190

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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 et 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 sac vomitoire avec sachet PRO, boîte de 20
UDI-DI code: 03760059239208
Basic UDI-DI: 376005923RECUEILEXCDT01AY
Reference / catalog number: 7733190
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: CareBag® bags, vomit bag with super absorbent bag, is made of a low density polyethylene (LDPE) bag and contains a super-absorbent, water-soluble sachet made of a PVOH film (polyvinyl alcohol) containing 10 g of Super-Absorbent Polymers (sodium polyacrylate) with an absorption capacity of 500 ml of 0.9% saline solution) intended for collection of vomit.
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.