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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

IC5600 — IVDD — General IVDD by ImmuChrom GmbH

MD Atlas
ImmuChrom GmbH

EUDAMED last updated this device on May 27, 2026

IC5600

B-04260154635602

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: ImmuChrom GmbH
UDI-DI code: 04260154635602
Reference / catalog number: IC5600

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View device family (Basic UDI)

Manufacturer information

Organization name: ImmuChrom GmbH
SRN: DE-MF-000033427
Manufacturer status: Active

Critical warnings

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

CW265
Stop solution contains acid

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Nov 22, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260154635602
Basic UDI-DI: B-04260154635602
Reference / catalog number: IC5600
Issuing entity: GS1

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: Photometric testkit for the quantitative determination of the beta-Glucuronidase activity in stool (96 tests)
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04260154635602

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

W01019099CLINICAL CHEMISTRY REAGENTS - OTHER

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

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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.