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

820/4x08 — Class I MDR by P.E.E.T.H.-PRODUTOS…

MD Atlas
P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA

EUDAMED last updated this device on May 13, 2026

820/4x08

560080609LIGSE7X

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA
UDI-DI code: 05600806091414
Reference / catalog number: 820/4x08

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: P.E.E.T.H.-PRODUTOS ELASTICOS ESPECIAIS E TENSORES HETERODINAMICOS LDA
SRN: PT-MF-000010370
Manufacturer status: Active

Related devices

1001560080609ALPOD5SOn the market 1002560080609ALPOD5SOn the market 1003560080609ALPOD5SOn the market 1011560080609ALPOD5SOn the market 1021560080609ALPOD5SOn the market

Critical warnings

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

CW999
Não aplicar a ligadura super elástica diretamente sobre feridas abertas ou em outras condições dermatológicas onde possa ocorrer infeção. Não aplicar a ligadura super elástica em membros corporais com problemas circulatórios de origem arterial.

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 Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05600806091414
Basic UDI-DI: 560080609LIGSE7X
Reference / catalog number: 820/4x08
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: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 8 MU10
4 MU36

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05600806091414

Sign in to download the DataMatrix

Create a free account to download the UDI-DI DataMatrix for this device.

Email

Password

No account yet?

UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

Sign in to generate the UDI-PI DataMatrix

Create a free account, then generate the compliant UDI-PI carrier for this device.

Email

Password

No account yet?

EMDN nomenclature code(s)

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

M0304010102ELASTIC COMPRESSION BANDAGES, NON-ADHESIVE, MEDIUM EXTENSIBILITY (70-140%)

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

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.