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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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HPM Roll-on cuff — 6 UDI-DI variants, MDR (Hammarplast Medical AB)

MD Atlas
Hammarplast Medical AB

Data from EUDAMED, last updated May 30, 2026

HPM Roll-on cuff

0734007791005TT

6 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: Hammarplast Medical AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 0734007791005TT
Device name: —
Device model: HPM Roll-on cuff
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Hammarplast Medical AB
SRN: SE-MF-000009420
Country: Sweden
Email: info@hpm.se
Phone: +4651061880

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KS26P12CCJV2GP2SX27Q62PN

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

Roll- on cuff 25-31 cm07340077901446
Roll- on cuff 30-38 cm07340077901453
Roll- on cuff 37-46 cm07340077901460
Roll- on cuff 45-56 cm07340077901477
Roll- on cuff 55-65 cm07340077901484
Roll- on cuff 64-80 cm07340077901491