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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

KD-Color GE10 — IVDD — General IVDD by KaliDiv

MD Atlas
KaliDiv

EUDAMED last updated this device on May 22, 2026

KD-Color GE10

B-03770040619070

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: KaliDiv
UDI-DI code: 03770040619070
Reference / catalog number: KDColorGE10

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Manufacturer information

Organization name: KaliDiv
SRN: FR-MF-000047430
Manufacturer status: Active

Critical warnings

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

CW010
Consult instructions for use
CW133
To avoid risks to human health and the environment, comply with the instructions for use.
CW032
Do not use past indicated date
CW036
Restrictions in use for combination of other devices
CW225
Absorb spillage to prevent material damage.
CW163
Do not eat, drink or smoke when using this product.
CW008
Biological risks
CW265
Contains hazardous substances
CW167
Wear protective gloves/protective clothing/eye protection/face protection.
CW160
Do not get in eyes, on skin, or on clothing.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: KD-Color GE10
UDI-DI code: 03770040619070
Basic UDI-DI: B-03770040619070
Reference / catalog number: KDColorGE10
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: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0104050102PARASITOLOGY STAINS

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

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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.