Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners 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

FCC50-1-2 — IVDD — General IVDD by FUTURLAB S.R.L.

MD Atlas
FUTURLAB S.R.L.

EUDAMED last updated this device on Mar 12, 2026

FCC50-1-2

B-CONTROLLO-NCY

On the marketIVDD — General

Applicable legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Organization name: FUTURLAB S.R.L.
UDI-DI code: D-CONTROLLO-NCY
Reference / catalog number: FCC50-1-2

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?

View device family (Basic UDI)

Manufacturer information

Organization name: FUTURLAB S.R.L.
SRN: IT-MF-000046539
Manufacturer status: Active

Related devices

FCC201-2B-ACIDI-BILIARI-TOTR8On the market FCC218-2B-ACIDO-URICO9GOn the market FCC219-2B-ALBUMINA-LRPAOn the market FCC213-2B-ALT-GPTZ3On the market FCC220B-AMILASE-LRGQOn 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.

Critical warnings

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

CW011
For in vitro diagnostic use. Handle according to good laboratory practice.

EasyUDICompliance engine

Sponsored

Your devices, UDI-compliant — without drowning in regulation

EUDAMED-ready· UDI-enriched

Basic UDIUDI-DIUDI-PIAttributeDocument

Print-ready label

From your product file — no manual entry

Exclusive to MD Atlas usersClaim my −20% discount

by Made In Tracker

Market distribution

Primary placement in Italy; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: D-CONTROLLO-NCY
Basic UDI-DI: B-CONTROLLO-NCY
Reference / catalog number: FCC50-1-2
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: CONTROL N is a multiparametric negative control material based on lyophilised human serum, intended exclusively for internal quality control of clinical chemistry tests. It is not intended to provide direct diagnostic information on the clinical status of the patient.
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

D-CONTROLLO-NCY

DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.

EMDN nomenclature code(s)

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

W0101050101ASSAYED MULTICOMPONENT CONTROLS (CC)

Compliance flags

Safety

Sterile

Single use

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Become a partner of MD Atlas