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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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COMPRESSE OROPHARYNGÉE — 2 UDI-DI variants, MDR (NICHROMINOX)

MD Atlas
NICHROMINOX

Data from EUDAMED, last updated May 19, 2026

COMPRESSE OROPHARYNGÉE

37014753OropacksNA

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: NICHROMINOX

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37014753OropacksNA
Device name: —
Device model: COMPRESSE OROPHARYNGÉE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: NICHROMINOX
SRN: FR-MF-000000181
Country: France
Email: office@nichrominox.fr
Phone: +33 (0)4 78 74 04 15

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KG2K5ZAAT12B2Y2A2D8V7SEM

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

PN09150003701475318948
PN091500XL03701475318931