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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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LimFlow V-Ceiver — 2 UDI-DI variants, MDR (LimFlow SA)

MD Atlas
LimFlow SA

Data from EUDAMED, last updated May 19, 2026

LimFlow V-Ceiver

0850017630VCCE21RS

2 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: LimFlow SA

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 1000261596
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: DQS Medizinprodukte GmbH (0297)
Validity: Aug 21, 2025 → Oct 26, 2028

Identity & classification

Basic UDI-DI: 0850017630VCCE21RS
Device name: LimFlow V-Ceiver
Device model: VC-CE-21
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 31, 2023

Manufacturer & authorised representative

Manufacturer

Name: LimFlow SA
SRN: FR-MF-000011529
Country: France
Email: info@limflow.com
Phone: +33.638.747.190

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HDRK9B7HD2VQ21JTCE8V0M6H

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

LimFlow V-Ceiver00850017630291
LimFlow V-Ceiver00850017630451