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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

12700 — IVDD — General IVDD by CellTrend GmbH

MD Atlas
CellTrend GmbH

EUDAMED last updated this device on Apr 24, 2026

12700

B-12700FA

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: CellTrend GmbH
UDI-DI code: D-12700FA
Reference / catalog number: 12700

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Manufacturer information

Organization name: CellTrend GmbH
SRN: DE-MF-000030872
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
CW266
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Feb 26, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: D-12700FA
Basic UDI-DI: B-12700FA
Reference / catalog number: 12700
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: EIA für die quantitative Bestimmung von IgG-Autoantikörper gegen den β2adrenergen Rezeptor (β2AR) im humanen Serum
Additional information URL: https://www.celltrend.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0102109099AUTO-IMMUNE DISEASE TESTS - 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

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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.