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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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EndoVcover sterile single use sheath — 5 UDI-DI variants, MDR

MD Atlas
V.I.M.S VIDEO INTERVENTIONNELLE MEDICALE SCIENTIFIQUE

Data from EUDAMED, last updated May 19, 2026

EndoVcover sterile single use sheath

376034603LWTF

5 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: V.I.M.S VIDEO INTERVENTIONNELLE MEDICALE SCIENTIFIQUE

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 376034603LWTF
Device name: EndoVcover sterile single use sheath
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 8, 2026

Manufacturer & authorised representative

Manufacturer

Name: V.I.M.S VIDEO INTERVENTIONNELLE MEDICALE SCIENTIFIQUE
SRN: FR-MF-000009063
Country: France
Email: contact.vims@zimmerbiomet.com
Phone: +33 5 34 45 09 09

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KK77MK6H6N6NE405SJVZM2F4

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

EndoVcover03760346035001
EndoVcover03760346031317
EndoVcover03760346034318
EndoVcover03760346035308
EndoVcover03760346031010