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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

GEUS-LB® — IVDD — General IVDD by ANILING SL

MD Atlas
ANILING SL

EUDAMED last updated this device on Mar 4, 2024

GEUS-LB®

B-8437025247GEUSLBC7

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: ANILING SL
UDI-DI code: D-8437025247GEUSLBC7
Reference / catalog number: GEUS-LB®

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Manufacturer information

Organization name: ANILING SL
SRN: ES-MF-000025687
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.

Market distribution

Primary placement in Spain; available across 1 country total.

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

Device identification

Trade name: GEUS-LB®
UDI-DI code: D-8437025247GEUSLBC7
Basic UDI-DI: B-8437025247GEUSLBC7
Reference / catalog number: GEUS-LB®
Issuing entity: EUDAMED

Classification

Risk category: IVDD — General
Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W01060299TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Related devices

GEUS-CLL®B-8437025247GEUS5QOn the market GEUS-CRC®B-8437025247GEUSCRCPDOn 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.