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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

DM1060520B — Class I MDR by Abílio Freire Lda

MD Atlas
Abílio Freire Lda

EUDAMED last updated this device on Dec 9, 2022

DM1060520B

5600710211DM106E6

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Abílio Freire Lda
UDI-DI code: 05600710211533
Reference / catalog number: DM1060520B

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Manufacturer information

Organization name: Abílio Freire Lda
SRN: PT-MF-000022553
Manufacturer status: Active

Related devices

DM1060515B5600710211DM106E6On the market DM1061515B5600710211DM106E6On the market DM1061010B5600710211DM106E6On the market DM1030515B5600710211DM103DYOn the market DM1030505B5600710211DM103DYOn 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.

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Placed on the market in Portugal; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 05600710211533
Basic UDI-DI: 5600710211DM106E6
Reference / catalog number: DM1060520B
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: 1
Additional product description: Ligadura de tecido de algodão (gaze). Destina-se a ser utilizado como barreira mecânica, de compressão ou ações de suporte.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 5 MU36
20 MU10

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M030101HYDROPHILIC GAUZE BANDAGES

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

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