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

LIG9000267 — Class I MDR by S.B.M. SAS

MD Atlas
S.B.M. SAS

EUDAMED last updated this device on Mar 25, 2025

LIG9000267

376015400DT2019049VZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: S.B.M. SAS
UDI-DI code: 03760154005708
Reference / catalog number: LIG9000267

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: S.B.M. SAS
SRN: FR-MF-000000214
Manufacturer status: Active

Related devices

PUL9000303376015400DT2019024VHOn the market 110026104376015400DT2019046VTOn the market 256412376015400DT2019046VTOn the market EPA9000303376015400DT2019024VHOn the market GLE9000409376015400DT2021011TTOn the market

Market distribution

Primary placement in France; available across 2 countries total.

Country	On market since	Until
FrancePrimary placement	Mar 1, 2015	Still on market
Spain	Sep 1, 2016	Still on market

Device identification

Trade name: not provided
UDI-DI code: 03760154005708
Basic UDI-DI: 376015400DT2019049VZ
Reference / catalog number: LIG9000267
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: Conical stopper
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L091099OSTEOSYNTHESIS INSTRUMENTS, REUSABLE - 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

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.