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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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SURVAC™ — 4 UDI-DI variants, MDR (NOVATECH SA)

MD Atlas
NOVATECH SA

Data from EUDAMED, last updated May 19, 2026

SURVAC™

4063108SURCB

4 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: NOVATECH SA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4063108SURCB
Device name: SURVAC™
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: NOVATECH SA
SRN: FR-MF-000001658
Country: France
Email: vigilance@novatech.fr
Phone: +33 442 98 15 60

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JQRN0XJZSKKVTZTQWHT76M72

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

7764214063108108668
7762214063108108644
7763214063108108651
77642SC14063108108675