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

1284 — Class I MDR by FARMABAN s.a.

MD Atlas
FARMABAN s.a.

EUDAMED last updated this device on Oct 7, 2025

1284

8428012COMPRESION2LRZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: FARMABAN s.a.
UDI-DI code: 08428012303063
Reference / catalog number: 1284

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: FARMABAN s.a.
SRN: ES-MF-000004713
Manufacturer status: Active

Related devices

ABSOHAFT8428012FIJACIONUBOn the market ABSOHAFT8428012FIJACIONUBOn the market ABSOHAFT8428012FIJACIONUBOn the market Absoplast8428012VF503-201ASOn the market Absoplast8428012VF503-201ASOn 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.

CW999
Dekompensierte Herzinsuffizienz Septische Phlebitis Fortgeschrittene diabetische Mikroangiopathie Phlegmasia coerulea dolens Schwewiegende arterielle Verschlusskrankheit bei patienten mit einem Knöchel-Arm-Index (ABI) von weniger als 0.6 Bekannte Überempfindlichkeit gegenüber einem der Bestandtele des Materials

Market distribution

Primary placement in Germany; available across 1 country total.

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

Device identification

Trade name: not provided
UDI-DI code: 08428012303063
Basic UDI-DI: 8428012COMPRESION2LRZ
Reference / catalog number: 1284
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 6
Additional product description: Mehrlagen-Kompressionssystem
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 10 MU10
5.5 MU36
18–25 MU10

EMDN nomenclature code(s)

M03040199ELASTIC COMPRESSION BANDAGES - 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

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification