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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

3873936 — Class I MDR by Laboratorios Indas, S.A.U

MD Atlas
Laboratorios Indas, S.A.U

EUDAMED last updated this device on Feb 4, 2026

3873936

5601227PANTYK

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratorios Indas, S.A.U
UDI-DI code: 05601227038156
Reference / catalog number: 3873936

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Manufacturer information

Organization name: Laboratorios Indas, S.A.U
SRN: ES-MF-000000586
Manufacturer status: Active

Related devices

38739205601227AALFU8On the market 38739215601227AALFU8On the market 38739185601227AALFU8On the market 387390156012270AEMGEDOn the market 387390256012270AEMGEDOn 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 Portugal; available across 2 countries total.

Country	On market since	Until
PortugalPrimary placement	Oct 30, 2019	Still on market
Spain	Oct 30, 2019	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05601227038156
Basic UDI-DI: 5601227PANTYK
Reference / catalog number: 3873936
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: 56
Additional product description: AMANHECER PANT T-M
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T04010103INCONTINENCE NAPPIES WITH INTEGRATED FIXING SYSTEM

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

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Expiration date
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