Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

AHLT_002 — IVDR Class A IVDR by biosurfit SA

MD Atlas
biosurfit SA

EUDAMED last updated this device on May 7, 2026

AHLT_002

56006094490AHLTTA2Z

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: 05600218925000
Reference / catalog number: AHLT_002

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

View device family (Basic UDI)

Manufacturer information

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

Related devices

AHLT_00656006094490AHLTTA2ZOn the market AHLT_00456006094490AHLTTU49On the market AHLT_00356006094490AHLTTRTA2JOn the market AHLT_00556006094490AHLTTUSH7On the market AHLT_00156006094490AHLTPEOn 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

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

CW010
EUDAMED did not publish a description for this code.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

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: 05600218925000
Basic UDI-DI: 56006094490AHLTTA2Z
Reference / catalog number: AHLT_002
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

Become a partner of MD Atlas