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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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Montures cerclées Plastique — 53 UDI-DI variants, MDR (ATOL GROUP)

MD Atlas
ATOL GROUP

Data from EUDAMED, last updated May 19, 2026

Montures cerclées Plastique

37016711FRPTY

53 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: ATOL GROUP

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37016711FRPTY
Device name: Montures cerclées Plastique
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: ATOL GROUP
SRN: FR-MF-000037164
Country: France
Email: j.xavier-mohane@atol.fr
Phone: +33380253400

Variants by status

UDI-DI variants

53 UDI-DI variants

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Applied filters

basicUdiUlid01HXRHS96EKD5JEHJAF7SDTCXH

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

ONEO03701671100194
ONEO03701671100316
ONEO03701671100224

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