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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

HB 2500 — IVDD — General IVDD by Diaglobal GmbH

MD Atlas
Diaglobal GmbH

EUDAMED last updated this device on Apr 8, 2026

HB 2500

B-4260152490623T2

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Diaglobal GmbH
UDI-DI code: D-4260152490623T2
Reference / catalog number: HB 2500

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Manufacturer information

Organization name: Diaglobal GmbH
SRN: DE-MF-000032608
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	May 1, 2000	Dec 30, 2029

Device identification

Trade name: not provided
UDI-DI code: D-4260152490623T2
Basic UDI-DI: B-4260152490623T2
Reference / catalog number: HB 2500
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: Reagenz zur Bestimmung von Hämoglobin im Blut
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0103010601HAEMOGLOBIN (HB)

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.