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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

TESTAmed GlucoCheck ADVANCED — IVDD — Annex II List B IVDD

MD Atlas
ForaCare Suisse AG

EUDAMED last updated this device on Oct 16, 2025

TESTAmed GlucoCheck ADVANCED

B-07640402713059

On the marketIVDD — Annex II List B

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: ForaCare Suisse AG
UDI-DI code: 07640402713059
Reference / catalog number: GD88

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Manufacturer information

Organization name: ForaCare Suisse AG
SRN: CH-MF-000019906
Manufacturer status: Active

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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.

Critical warnings

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

CW010
Consult instructions for use

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: TESTAmed GlucoCheck ADVANCED
UDI-DI code: 07640402713059
Basic UDI-DI: B-07640402713059
Reference / catalog number: GD88
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: Meter, EN manual, DE manual, TR manual, user guide, log book, warranty, lancing device, lancing device manual, 10pcs blood glucose strip, strip manual, lv2 control solution, control solution manual, lancet 10pcs, meter bag
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0201060102BLOOD GLUCOSE METERS

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

UDI-PI traceability

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