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

Proteus OXK, 20 x 5 mL — IVDD — General IVDD

MD Atlas
Chronolab Systems, S.L.

EUDAMED last updated this device on Oct 14, 2025

Proteus OXK, 20 x 5 mL

B-084360385345348FH

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: Chronolab Systems, S.L.
UDI-DI code: D-084360385345348FH
Reference / catalog number: 101-0072

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: Chronolab Systems, S.L.
SRN: ES-MF-000017043
Manufacturer status: Active

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.

Critical warnings

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

CW011
R: EUH208-Contains formaldehyde. May produce an allergic reaction. EUH210-Safety data sheet available on request Control + / - : H317-May cause an allergic skin reaction. Contain 2-Methylisothiazol- 3(2H)-one (Proclin 950). Follow the precautionary advice given in the SDS and the product label.

Market distribution

Primary placement in Spain; available across 1 country total.

Placed on the market in Spain; per-country availability dates not published.

Device identification

Trade name: Proteus OXK, 20 x 5 mL
UDI-DI code: D-084360385345348FH
Basic UDI-DI: B-084360385345348FH
Reference / catalog number: 101-0072
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: Kit content: Reagent, Positive control, Negative control All components are ready to use. Additional equipment needed: Standard laboratory equipment.
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

W0105011712PROTEUS

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

Acid phosphatase, 18 x 2 mLB-084360386006008CTOn the market Acid phosphatase, 4 x 50 mLB-084360388038031F7On the market Agglutination slide and tube tests with positive and negative controls, 8 x 5 mL, 2 x 1 mLB-084360386316313EMOn the market Albumin, 3 x 100 mLB-084360385725728GVOn the market Albumin, 4 x 250 mL

B-084360385395393HD

On the market