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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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Erisma LP — 1 UDI-DI variant, MDD (Clariance)

MD Atlas
Clariance

Data from EUDAMED, last updated May 31, 2026

Erisma LP

B-03700780605026

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIb

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Clariance

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Device characteristics

Implantable

Clinical investigations

Registered: No

Legacy certificates

Certificate number: 240656-2017-CE-FRA-NA-PS Rev.
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DNV Product Assurance AS (2460)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-03700780605026
Device name: Erisma LP
Device model: MONOAXIAL SCREW
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Clariance
SRN: FR-MF-000023666
Country: France
Email: q.tran@clariance-spinevision.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KSJ12VA743WMSJ3Z9839YC62

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

MONOAXIAL SCREW03700780605026