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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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Organization name
UDI-DI code
Reference / catalog number

LISA - Tensionner — Class I MDR by BACKBONE

MD Atlas
BACKBONE

EUDAMED last updated this device on Apr 30, 2026

LISA - Tensionner

376024863LISA230G7

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BACKBONE
UDI-DI code: 03760248630175
Reference / catalog number: BB-LISA-2-230

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Manufacturer information

Organization name: BACKBONE
SRN: FR-MF-000001874
Manufacturer status: Active

Related devices

LISA - Addiditional wrench376024863LISA241GCOn the market LISA - Band forceps I376024863LISA213G7On the market LISA - Band forceps II376024863LISA214G9On the market LISA - Gripper Screwdriver376024863LISA250GDOn the market LISA - Hook376024863LISA215GBOn the market

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
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: LISA - Tensionner
UDI-DI code: 03760248630175
Basic UDI-DI: 376024863LISA230G7
Reference / catalog number: BB-LISA-2-230
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: https://elabeling.companion-spine.com/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

L091199ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER
L1299LAPAROSCOPIC AND THORACOSCOPIC 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.