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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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NOVASTRAP — 6 UDI-DI variants, MDR (NOVATEX MEDICAL SA)

MD Atlas
NOVATEX MEDICAL SA

Data from EUDAMED, last updated May 19, 2026

NOVASTRAP

37014229NOVASTRAPND

6 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: NOVATEX MEDICAL SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 37014229NOVASTRAPND
Device name: NOVASTRAP
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 11, 2024

Manufacturer & authorised representative

Manufacturer

Name: NOVATEX MEDICAL SA
SRN: FR-MF-000014276
Country: France
Email: contact@novatex-medical.com
Phone: +33374010397

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01HRQ4M6EBB92HC51CKVS58FZQ

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

0370142290004203701422900042
0370142290000403701422900004
0370142290003503701422900035
0370142290005903701422900059
0370142290002803701422900028
0370142290001103701422900011