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

FTP042 — Class IIa MDD by Labomar S.p.A.

MD Atlas
Labomar S.p.A.

EUDAMED last updated this device on Apr 13, 2026

FTP042

B-FTP042EM

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Labomar S.p.A.
UDI-DI code: D-FTP042EM
Reference / catalog number: FTP042

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: Labomar S.p.A.
SRN: IT-MF-000007965
Manufacturer status: Active

Related devices

FTP035B-FTP035_1JLOn the market FTP089B-FTP089_1LBOn the market FTPR101805630062FTPR101DKOn the market FTPR101805630062FTPR101DKOn the market FTPR101805630062FTPR101DKOn the market

Certificates

Certificate health across this manufacturer's portfolio.

CSQ0026240424Supplemented
Quality management systemNotified body: 0373Expiry: Oct 27, 2029

Critical warnings

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

CW999
Do not use on infected, large or deep wounds. Do not use in case of allergy or hypersensitivity to any component. Do not swallow. Stop the treatment in case of abnormal skin reactions. Avoid contact with eyes, in case of contact, immediately wash your eyes with water. Do not use in case the package is open or damaged. Carefully close the tube after use. Keep out of the reach of children. External use, do not swallow. Do not use after the expiry date reported on the package. The expiry date refers to the product properly stored in unopened package.

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 Poland; available across 1 country total.

Country	On market since	Until
PolandPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: D-FTP042EM
Basic UDI-DI: B-FTP042EM
Reference / catalog number: FTP042
Issuing entity: EUDAMED

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: ARGOTIAB Rapid hydrogel is a medical device for the treatment of superficial wounds, abrasions, excoriations and chaps. It is also indicated for the treatment of acute phases and relapses of atopic dermatitis, dermatitis in general, eczema, particularly irritated skin characterized by micro-lesions
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

EMDN nomenclature code(s)

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

V9099VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

Become a partner of MD Atlas