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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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Venoline 140 den — 15 UDI-DI variants, MDR (Inverdia AB)

MD Atlas
Inverdia AB

Data from EUDAMED, last updated May 31, 2026

Venoline 140 den

73310044323C

15 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: Inverdia AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73310044323C
Device name: Venoline 140 den
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Inverdia AB
SRN: SE-MF-000047520
Country: Sweden
Email: info@inverdia.com
Phone: +4686275044

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KPZQHQMR22HZE5JFYEVHKKEJ

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

Venoline 140 den07331004432218
Venoline 140 den07331004432317
Venoline 140 den07331004432133
Venoline 140 den07331004432324
Venoline 140 den07331004432539
Venoline 140 den07331004432126
Venoline 140 den07331004432331
Venoline 140 den07331004432119
Venoline 140 den07331004432430
Venoline 140 den07331004432515
Venoline 140 den07331004432423
Venoline 140 den07331004432416
Venoline 140 den07331004432225
Venoline 140 den07331004432232
Venoline 140 den07331004432522