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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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Septinasal single dose — 3 UDI-DI variants, MDR (GIFRER BARBEZAT)

MD Atlas
GIFRER BARBEZAT

Data from EUDAMED, last updated May 19, 2026

Septinasal single dose

37011290FR00257

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: GIFRER BARBEZAT

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37011290FR00257
Device name: Septinasal single dose
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: GIFRER BARBEZAT
SRN: FR-MF-000011164
Country: France
Email: lydia.grabarczyk@gifrer.fr
Phone: 0604700854

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KNS10KZTKKM9FT8S9FK9HMFK

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

6000057815908311593438
PHYSIOLOGICA SEPTINASAL13701129005405
Septinasal unidoses13701129004019