Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

CQI KD-Col/PM/Susp-G.d K — IVDD — General IVDD by KaliDiv

MD Atlas
KaliDiv

EUDAMED last updated this device on May 22, 2026

CQI KD-Col/PM/Susp-G.d K

B-03770040619124

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: KaliDiv
UDI-DI code: 03770040619124
Reference / catalog number: Mt11Gd21

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

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

Critical warnings

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

CW058
Flammable liquid and vapour.
CW095
Suspected of causing cancer.
CW085
Causes serious eye irritation.
CW082
Causes skin irritation.
CW083
May cause an allergic skin reaction.
CW139
Keep away from heat/sparks/open flames/hot surfaces. — No smoking.
CW138
Do not handle until all safety precautions have been read and understood.
CW168
Use personal protective equipment as required.
CW304
If eye irritation persists: Get medical advice/attention.
CW313
IF exposed or concerned: Get medical advice/attention.
CW163
Do not eat, drink or smoke when using this product.
CW162
Wash thoroughly after handling.
CW164
Use only outdoors or in a well-ventilated area.
CW167
Wear protective gloves/protective clothing/eye protection/face protection.
CW160
Do not get in eyes, on skin, or on clothing.
CW159
Avoid breathing dust/fume/gas/mist/vapours/spray.
CW401
IF INHALED: Remove victim to fresh air and keep at rest in a position comfortable for breathing.
CW422
IF ON SKIN: Wash with plenty of soap and water.
CW305
If skin irritation occurs: Get medical advice/attention.
CW416
IF IN EYES: Rinse cautiously with water for several minutes.
CW193
IF SWALLOWED: Rinse mouth.
CW307
IF SWALLOWED: Get medical advice/attention.
CW166
Avoid release to the environment.
CW133
To avoid risks to human health and the environment, comply with the instructions for use.

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: CQI KD-Col/PM/Susp-G.d K
UDI-DI code: 03770040619124
Basic UDI-DI: B-03770040619124
Reference / catalog number: Mt11Gd21
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)

W01040699CONTROLS, STANDARDS, CALIBRATORS, MICROBIOLOGY - 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

Related devices

CQI KD-Col/PM/L-Cryptosporidies3770040619CRYPTOSPOLAMEFEOn the market CQI KD-Col/PM/L-CryptosporidiesB-03770040619094On the market CQI KD-Col/PM/Susp-E.h FvB-03770040619100On the market CQI KD-Col/PM/Susp-E.h Fv3770040619SUSPARACOLOQXOn the market CQI KD-Col/PM/Susp-E.hmd Fv3770040619SUSPARACOLOQXOn 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.