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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

M 400062 — Class I MDD by L.A. Medical -…

MD Atlas
L.A. Medical - Fabricantes de Instrumentos Cirúrgicos, Lda

EUDAMED last updated this device on Jun 14, 2022

M 400062

B-05607858000098

On the marketClass I

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: L.A. Medical - Fabricantes de Instrumentos Cirúrgicos, Lda
UDI-DI code: 05607858000098
Reference / catalog number: M 400062

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View device family (Basic UDI)

Manufacturer information

Organization name: L.A. Medical - Fabricantes de Instrumentos Cirúrgicos, Lda
SRN: PT-MF-000012713
Manufacturer status: Active

Critical warnings

No critical warnings reported for this device.

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Market distribution

Primary placement in Portugal; available across 3 countries total.

Country	On market since	Until
PortugalPrimary placement		Still on market
Spain		Still on market
France		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05607858000098
Basic UDI-DI: B-05607858000098
Reference / catalog number: M 400062
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Chave de parafusos, 3.5mm hexagonal, 27.5cm compr.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05607858000098

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EMDN nomenclature code(s)

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

L0999ORTHOPAEDIC AND TRAUMATOLOGICAL SURGERY INSTRUMENTS, REUSABLE - OTHER
L99SURGICAL INSTRUMENTS, REUSABLE - OTHER

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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Related devices

This device is not currently linked to any other device.

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.