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

754114 — Class I MDR by Laboratoire SYLAMED

MD Atlas
Laboratoire SYLAMED

EUDAMED last updated this device on Feb 4, 2025

754114

3664666SPARADRAPFIXATE4

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Laboratoire SYLAMED
UDI-DI code: 03664666001114
Reference / catalog number: 754114

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

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

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 2 countries total.

Country	On market since	Until
FrancePrimary placement		Still on market
Germany		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03664666001114
Basic UDI-DI: 3664666SPARADRAPFIXATE4
Reference / catalog number: 754114
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: 10 m x 20 cm

EMDN nomenclature code(s)

M050201EXTENSIBLE NON-WOVEN PLASTERS

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

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