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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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Sterile non woven swabs — 3 UDI-DI variants, MDR (Laboratoire SYLAMED)

MD Atlas
Laboratoire SYLAMED

Data from EUDAMED, last updated May 19, 2026

Sterile non woven swabs

3664666CNTS7W

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Laboratoire SYLAMED

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 3664666CNTS7W
Device name: Sterile non woven swabs
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Laboratoire SYLAMED
SRN: FR-MF-000000361
Country: France
Email: info@sylamed.fr
Phone: +33148789739

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KMJRCSZ9QYXKQ5CA8DB9Z2Y9

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Compresses en non-tissé stériles03664666111394
Compresses stériles non tissées STERIPAN03664666014862
Compresses stériles non tissées STERIPAN03664666014909