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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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SAM·MAS MANDIBULAR ADVANCEMENT… — 2 UDI-DI variants, MDR

MD Atlas
VEC MEDICAL SPAIN, S.L.

Data from EUDAMED, last updated May 23, 2026

SAM·MAS MANDIBULAR ADVANCEMENT SELECTOR

84365702328TE

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: VEC MEDICAL SPAIN, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84365702328TE
Device name: SAM·MAS MANDIBULAR ADVANCEMENT SELECTOR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 6, 2025

Manufacturer & authorised representative

Manufacturer

Name: VEC MEDICAL SPAIN, S.L.
SRN: ES-MF-000002992
Country: Spain
Email: eudamed@vecmedical.com
Phone: +34 935 72 50 15

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01K6WY1RJNBE6XYEGG8V5A7YA7

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

LEFT SAM·MAS KIT08436570232183
RIGHT SAM·MAS KIT08436570232190