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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

AHLT_001 — IVDR Class A IVDR by biosurfit SA

MD Atlas
biosurfit SA

EUDAMED last updated this device on May 7, 2026

AHLT_001

56006094490AHLTPE

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: biosurfit SA
UDI-DI code: 05600609449085
Reference / catalog number: AHLT_001

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View device family (Basic UDI)

Manufacturer information

Organization name: biosurfit SA
SRN: PT-MF-000033920
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement	Nov 2, 2022	Still on market

Device identification

Trade name: not provided
UDI-DI code: 05600609449085
Basic UDI-DI: 56006094490AHLTPE
Reference / catalog number: AHLT_001
Issuing entity: GS1

Classification

Risk category: IVDR Class A
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: The Lab in the Box kit is a single-use in vitro diagnostic device that allows for the self-collection and storage of human biological samples and subsequent transport of the sample for laboratory analysis. This kit can be used for the collection, transport, and laboratory analysis of a range of parameters. The use of this kit alone is not appropriate for screening, monitoring, or diagnosis. The kit is a collection device suitable for lay users over the age of 18. There is no automation or quantification involved.
Additional information URL: https://labinthebox.pt/en
Clinical sizes: No clinical sizes registered for this device.

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.

W0501010280CAPILLARY BLOOD COLLECTION DEVICES - ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.