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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

TENDER ULTRA CARE LARGE No.3 DAY… — Class I MDR

MD Atlas
C.A. PAPAELLINAS LTD

EUDAMED last updated this device on Apr 24, 2026

TENDER ULTRA CARE LARGE No.3 DAY 30'S

5290013DIAPERSKB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: C.A. PAPAELLINAS LTD
UDI-DI code: 05290013022402
Reference / catalog number: 1026595

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Manufacturer information

Organization name: C.A. PAPAELLINAS LTD
SRN: CY-MF-000045516
Manufacturer status: Active

Critical warnings

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

CW009
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Cyprus; available across 1 country total.

Country	On market since	Until
CyprusPrimary placement	May 20, 2025	Still on market

Device identification

Trade name: TENDER ULTRA CARE LARGE No.3 DAY 30'S
UDI-DI code: 05290013022402
Basic UDI-DI: 5290013DIAPERSKB
Reference / catalog number: 1026595
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: 30
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 100–150 MU10

EMDN nomenclature code(s)

T04010102SHAPED INCONTINENCE NAPPIES

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.