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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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ABILITY STANDARD CUFF SET — 12 UDI-DI variants, MDR (ArjoHuntleigh AB)

MD Atlas
ArjoHuntleigh AB

Data from EUDAMED, last updated May 31, 2026

ABILITY STANDARD CUFF SET

5060693520433WA

12 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: ArjoHuntleigh AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5060693520433WA
Device name: ABILITY STANDARD CUFF SET
Device model: ACC-VAS-006
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 14, 2025

Manufacturer & authorised representative

Manufacturer

Name: ArjoHuntleigh AB
SRN: SE-MF-000000696
Country: Sweden
Email: info@arjo.com
Phone: +46 10 335 4500

Variants by status

UDI-DI variants

12 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KA0Z573HJ0BYGBQPT9AVH7YK

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

ACC-VAS-00605051968030320
ACC-VAS-00905051968030351
ACC-VAS-00705051968030337
ACC-VAS-00805051968030344
ACC-VAS-01005051968030368
ACC-VAS-01105051968030375
ACC-VAS-02705051968030511
ACC-VAS-01605051968030412
ACC-VAS-02605051968030504
ACC-VAS-02505051968030498
ACC-VAS-02305051968030474
ACC-VAS-02405051968030481