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

DECOCENT — IVDR Class A IVDR by DIAGNOTIS SAS

MD Atlas
DIAGNOTIS SAS

EUDAMED last updated this device on Jul 22, 2025

DECOCENT

3770032939DCC050S4

On the marketIVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Organization name: DIAGNOTIS SAS
UDI-DI code: 03770032939094
Reference / catalog number: DCC050

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: DIAGNOTIS SAS
SRN: FR-MF-000035861
Manufacturer status: Active

Related devices

DCC0513770032939DCC051S6On the market DECOMICS3770032939DEC010SEOn the market MPS2303770032939MPS2305XOn the market TM2403770032939TM240Y5On the market MPS230-SP13770032939MPS230-SP1MYOn the market

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Jul 22, 2025	Still on market
Portugal	Jul 22, 2025	Still on market

Device identification

Trade name: DECOCENT
UDI-DI code: 03770032939094
Basic UDI-DI: 3770032939DCC050S4
Reference / catalog number: DCC050
Issuing entity: GS1

Classification

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

Device details

Quantity: 1
Additional product description: DECOCENT® is a sample decontamination and concentration kit. It permits the processing of samples for microscopy, culture and molecular methods, for identification and isolation of mycobacteria. It is intended for in vitro diagnostic use.
Additional information URL: https://diagnotis.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0105010799MYCOBACTERIA REAGENTS - 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

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.