Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Kuntoilu- ja kuntoutuslaitteet — 11 UDI-DI variants, MDR (Ab HUR Oy)

MD Atlas
Ab HUR Oy

Data from EUDAMED, last updated May 23, 2026

Kuntoilu- ja kuntoutuslaitteet

642981020311627G4

11 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: Ab HUR Oy

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 642981020311627G4
Device name: Kuntoilu- ja kuntoutuslaitteet
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 23, 2022

Manufacturer & authorised representative

Manufacturer

Name: Ab HUR Oy
SRN: FI-MF-000008012
Country: Finland
Email: sales@hur.fi
Phone: +35868325500

Variants by status

UDI-DI variants

11 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01GMZ3JZCA9Q0R41EQ9Z31C3QW

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

5140 Chest Press Rehab06429810203342
5160 Pec Deck Rehab06429810203359
9140 Chest Press Easy Access06429810203489
9160 Pec Deck Easy Access06429810203502
ST5140-Hi5-MD Chest Press06429810203069
ST5160-Hi5-MD Pec Deck06429810203083
ST9140-Hi5-MD Chest Press Easy Access06429810203236
ST9160-Hi5-MD Pec Deck Easy Access06429810203250
STE5140-Hi5-MD Chest Press06429810203076
STE5140-Hi5-MD-P Chest Press06429810203847
STE5160-Hi5-MD06429810203090