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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

WE200.08 — IVDR Class A IVDR by Gold Standard…

MD Atlas
Gold Standard Diagnostics Frankfurt GmbH

EUDAMED last updated this device on Nov 13, 2024

WE200.08

++ENTIWE20008V037L

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Gold Standard Diagnostics Frankfurt GmbH
UDI-DI code: +ENTIWE2000809
Reference / catalog number: WE200.08

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Manufacturer information

Organization name: Gold Standard Diagnostics Frankfurt GmbH
SRN: DE-MF-000025020
Manufacturer status: Active

Critical warnings

8 warnings recorded — scroll inside the panel to see all entries.

CW043
EUDAMED did not publish a description for this code.
CW083
EUDAMED did not publish a description for this code.
CW106
EUDAMED did not publish a description for this code.
CW159
EUDAMED did not publish a description for this code.
CW166
EUDAMED did not publish a description for this code.
CW167
EUDAMED did not publish a description for this code.
CW306
EUDAMED did not publish a description for this code.
CW116
EUDAMED did not publish a description for this code.

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: not provided
UDI-DI code: +ENTIWE2000809
Basic UDI-DI: ++ENTIWE20008V037L
Reference / catalog number: WE200.08
Issuing entity: HIBCC

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

EMDN nomenclature code(s)

W0105900201BUFFERS (UNASSIGNABLE ), SUPPLEM. REAGENTS, ETC

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

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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.