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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Bandes extensibles UP — Class I MDR by Laboratoire SYLAMED

MD Atlas
Laboratoire SYLAMED

EUDAMED last updated this device on Mar 25, 2026

Bandes extensibles UP

3664666BANDEEXTENSIBLEW3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoire SYLAMED
UDI-DI code: 03401060029715
Reference / catalog number: 6002971

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Manufacturer information

Organization name: Laboratoire SYLAMED
SRN: FR-MF-000000361
Manufacturer status: Active

Related devices

Bande adhésive élastique ALVITA3664666BANDEADHESIVEXGOn the market Bande adhésive élastique ALVITA3664666BANDEADHESIVEXGOn the market Bande adhésive élastique ALVITA3664666BANDEADHESIVEXGOn the market Bande adhésive élastique MARQUE CONSEIL3664666BANDEADHESIVEXGOn the market Bande adhésive élastique MARQUE CONSEIL3664666BANDEADHESIVEXGOn the market

Critical warnings

2 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

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

Device identification

Trade name: Bandes extensibles UP
UDI-DI code: 03401060029715
Basic UDI-DI: 3664666BANDEEXTENSIBLEW3
Reference / catalog number: 6002971
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: 4m x 10cm

EMDN nomenclature code(s)

M0303010101ELASTIC FIXING BANDAGES, NON-ADHESIVE, EXTENSIBLE IN ONE DIRECTION

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

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.