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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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Rectal Cannula — 3 UDI-DI variants, MDR (SYMATESE DEVICE)

MD Atlas
SYMATESE DEVICE

Data from EUDAMED, last updated May 19, 2026

Rectal Cannula

376024313CANULERECTALEJN

3 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: SYMATESE DEVICE

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 376024313CANULERECTALEJN
Device name: Rectal Cannula
Device model: 0202
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 26, 2024

Manufacturer & authorised representative

Manufacturer

Name: SYMATESE DEVICE
SRN: FR-MF-000020651
Country: France
Email: reglementaire.r&d@symatesedevice.com
Phone: +33472397414

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J19P3TJ4BJPV8J5BD4Y2RTHF

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

Rectal Cannula03760243130175
Rectal Cannula03760243130199
Rectal Cannula03760243130038