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Organization name
UDI-DI code
Reference / catalog number

CAREBAG Baby, Potty Liner — Class I MDR by CLEANIS

MD Atlas
CLEANIS

EUDAMED last updated this device on Nov 17, 2025

CAREBAG Baby, Potty Liner

376005923RECUEILEXCDT01AY

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CLEANIS
UDI-DI code: 03760059232162
Reference / catalog number: 7711190

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Manufacturer information

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

Critical warnings

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

CW416
EUDAMED did not publish a description for this code.
CW009
EUDAMED did not publish a description for this code.
CW277
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW135
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: CAREBAG Baby, Potty Liner
UDI-DI code: 03760059232162
Basic UDI-DI: 376005923RECUEILEXCDT01AY
Reference / catalog number: 7711190
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 BABY is a Potty liner withdrawstring ties containing a super absorbent pad (Absorption capacity:200ml/7oz of 0.9% saline solution equivalent) intended for the collection of excreta. Precautions for use Single use. If reused, there is a risk of insufficient or no absorption and therefore potential contamination and is comfort for the patient. In case the eyes and mucous membranes come in contact with the pad, rinse well with water. In the event of persistent discomfort, contact your doctor. Adult supervision is required for use. Do not detach the pad from the bag. Do not allow contact with damaged skin. Keep out of the reach of children. Storage and disposal The product must be protected from moisture and kept away from sunlight. Dispose of in house holdwaste or according to the waste management protocol in force in the facility.
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.