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

TROUSSE EXTREMITE — Class I MDR by LABORATOIRES EUROMEDIS

MD Atlas
LABORATOIRES EUROMEDIS

EUDAMED last updated this device on Sep 12, 2025

TROUSSE EXTREMITE

33893681DJ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: LABORATOIRES EUROMEDIS
UDI-DI code: 23389360014980
Reference / catalog number: 164103

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: LABORATOIRES EUROMEDIS
SRN: FR-MF-000036597
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.
CW001
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: TROUSSE EXTREMITE
UDI-DI code: 23389360014980
Basic UDI-DI: 33893681DJ
Reference / catalog number: 164103
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: No clinical sizes registered for this device.

EMDN nomenclature code(s)

T0202SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)

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

Casaque chirurgicale standard plus + 2 essuie-mains (Taille L)33893661DCOn the market Casaque chirurgicale standard plus + 2 essuie-mains (Taille XLL)33893661DCOn the market Casaque chirurgicale stérile renforcée + 2 essuie-mains (Taille L) Dimensions : 130±2 X 160±2 cm33893662DEOn the market Casaque chirurgicale stérile renforcée + 2 essuie-mains (Taille XL) Dimensions : 140±2 X 160±2 cm33893662DEOn the market

Casaque chirurgicale stérile renforcée + 2 essuie-mains (Taille XLL) Dimensions : 150±2 X 160±2 cm

33893662DE

On the market