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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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LINGOT CERABALT K30 — 3 UDI-DI variants, MDR (BERNARD CERVOS SOCIETE)

MD Atlas
BERNARD CERVOS SOCIETE

Data from EUDAMED, last updated May 19, 2026

LINGOT CERABALT K30

376035797K30JA

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: BERNARD CERVOS SOCIETE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376035797K30JA
Device name: LINGOT CERABALT K30
Device model: CERABALT K30
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 23, 2021

Manufacturer & authorised representative

Manufacturer

Name: BERNARD CERVOS SOCIETE
SRN: FR-MF-000016213
Country: France
Email: moucherfi@acnis-titanium.com
Phone: +33 4 72 21 42 90

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01FQK7A6WQ3DQ7EXCNB3S99T9Q

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

CERABALT K3003760357970025
CERABALT K30 GRENAILLE03760357970223
CERABALT K30 Neutre03760357974030