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

1220LSU1B-3200 — Class IIa MDR by EUROMI

MD Atlas
EUROMI

EUDAMED last updated this device on May 20, 2026

1220LSU1B-3200

3701416250000CAN3G

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: EUROMI
UDI-DI code: 03701416203883
Reference / catalog number: 1220LSU1B-3200

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: EUROMI
SRN: BE-MF-000014212
Manufacturer status: Active

Critical warnings

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

CW999
Inspect the sterile components to ensure their packaging is not damaged. Do not use the device if package is damaged.
CW999
Always visually inspect each cannula before use. Discard the cannula if there are any signs of wear, cracking, corrosion, or if the cannula is bent, broken or deformed.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	May 20, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03701416203883
Basic UDI-DI: 3701416250000CAN3G
Reference / catalog number: 1220LSU1B-3200
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: CANULE DE REINJECTION MANUELLE A USAGE UNIQUE MODELE 1B DIAMETRE 3 LONGUEUR 200
Additional information URL: https://www.euromi.com/fr/doc-professionnelle/
Clinical sizes: 200 MU50
3 MU50

EMDN nomenclature code(s)

V901699SPECIALIST SURGICAL INSTRUMENTS AND KITS NOT INCLUDED IN OTHER CLASSES, SINGLE-USE - OTHER

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

1316INFL-2.51503701416250000CAN3GOn the market 1118NLF2DH3701416280000NLF7HOn the market 1127ADIPC3701416260000EVA5JOn the market

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.