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

L2M-MKT-LMT — Class III MDD by L2MTech GmbH

MD Atlas
L2MTech GmbH

EUDAMED last updated this device on Mar 26, 2024

L2M-MKT-LMT

B-04262473120210

On the marketClass III

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: L2MTech GmbH
UDI-DI code: 04262473120210
Reference / catalog number: L2M-MKT-LMT

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: L2MTech GmbH
SRN: DE-MF-000036711
Manufacturer status: Active

Critical warnings

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

CW010
EUDAMED did not publish a description for this code.
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 Spain; available across 3 countries total.

Country	On market since	Until
SpainPrimary placement		Still on market
Austria		Still on market
Czechia		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262473120210
Basic UDI-DI: B-04262473120210
Reference / catalog number: L2M-MKT-LMT
Issuing entity: GS1

Classification

Risk category: Class III
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Sirolimus Eluting Cobalt chromium coronary stent system
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

P070402010301CORONARY DRUG ELUTING STENTS (DES) WITH POLYMERS

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

LomiFlowB-04262375060003On 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.