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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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Vein strippers — 8 UDI-DI variants, MDR (Telic, S.A.U.)

MD Atlas
Telic, S.A.U.

Data from EUDAMED, last updated May 23, 2026

Vein strippers

8427734VEINSTRIPPERSZP

8 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: Telic, S.A.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8427734VEINSTRIPPERSZP
Device name: Vein strippers
Device model: VE-022
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Jul 18, 2024

Manufacturer & authorised representative

Manufacturer

Name: Telic, S.A.U.
SRN: ES-MF-000001853
Country: Spain
Email: info@telic.es
Phone: 00 34 93 865 61 25

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01J1PDAD0EAT2KM21E0472R2AF

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

VE-02208427734039564
VE-02208427734035382
VE-02208427734028186
VE-02208427734031889
VE-02508427734032442
VE-02508427734000984
VE-022 OP08427734010648
TCS0108427734000953