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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

001 — IVDR Class C IVDR by Institut für Klinische…

MD Atlas
Institut für Klinische Transfusionsmedizin und Immungenetik Ulm gemeinnützige GmbH

EUDAMED last updated this device on Jul 15, 2025

001

++G286HSeqABCKR

On the marketIVDR Class C

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: Institut für Klinische Transfusionsmedizin und Immungenetik Ulm gemeinnützige GmbH
UDI-DI code: +G2860010V
Reference / catalog number: 001

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Manufacturer information

Organization name: Institut für Klinische Transfusionsmedizin und Immungenetik Ulm gemeinnützige GmbH
SRN: DE-MF-000018980
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: +G2860010V
Basic UDI-DI: ++G286HSeqABCKR
Reference / catalog number: 001
Issuing entity: HIBCC

Classification

Risk category: IVDR Class C
Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: H-Seq-ABC ist ein In vitro Diagnostikum, das für die hochauflösende Typisierung der HLA-Merkmale A, B und C eingesetzt wird
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0106010401HLA-TYPING
W01030403HLA ANTIGEN TYPING

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

014++G286HSeqNGSP9On 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.