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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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XO ODONTOSURGE — 1 UDI-DI variant, MDD (XO CARE A/S)

MD Atlas
XO CARE A/S

Data from EUDAMED, last updated May 31, 2026

XO ODONTOSURGE

B-XOOSUBL

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: XO CARE A/S

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Device characteristics

Active deviceReusable

Legacy certificates

Certificate number: 241352-2017-CE-NOR-NA-PS
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-XOOSUBL
Device name: XO ODONTOSURGE
Device model: XO ODONTOSURGE 4
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 23, 2023

Manufacturer & authorised representative

Manufacturer

Name: XO CARE A/S
SRN: DK-MF-000003605
Country: Denmark
Email: regulatory@xo-care.com

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GQFG2M6S95KPYGM1T3TZXDWG

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

XO ODONTOSURGED-XOOSUBL