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.

ASTER ELECTRIC — 15 UDI-DI variants, MDR (Reha-Bed Sp. z o.o.)

MD Atlas
Reha-Bed Sp. z o.o.

Data from EUDAMED, last updated May 30, 2026

ASTER ELECTRIC

59041832ASTERELSW

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: Reha-Bed Sp. z o.o.

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?

UDI-DI variants

15 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

basicUdiUlid01KADKWXKN9FB68HWGW5E9WJBS

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

ASTER RECLINER ELECTRIC CADET ZEST 110 PACIFIC05904183222905
ASTER RECLINER ELECTRIC CADET ZEST 124 ELECTRIC BLUE05904183222912
ASTER RECLINER ELECTRIC CADET ZEST 201 JADE05904183222929
ASTER RECLINER ELECTRIC CADET ZEST 219 SEAFOAM05904183222936
ASTER RECLINER ELECTRIC CADET ZEST 238 CITRUS05904183222943
ASTER RECLINER ELECTRIC CADET ZEST 303 LEMON05904183222950
ASTER RECLINER ELECTRIC CADET ZEST 314 MUSTARD05904183222967
ASTER RECLINER ELECTRIC CADET ZEST 440 SCARLET05904183222974
ASTER RECLINER ELECTRIC CADET ZEST 608 FUCHSIA05904183222981
ASTER RECLINER ELECTRIC CADET ZEST 646 PEONY05904183222998
ASTER RECLINER ELECTRIC CADET ZEST 805 CREAM05904183223001
ASTER RECLINER ELECTRIC CADET ZEST 901 SILVER05904183223018
ASTER RECLINER ELECTRIC PIANO 1505904183223025
ASTER RECLINER ELECTRIC VIENNA 04 CAPPUCINO05904183223032
ASTER RECLINER ELECTRIC VIENNA 15 PLATINUM05904183223049

Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59041832ASTERELSW
Device name: ASTER ELECTRIC
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Reha-Bed Sp. z o.o.
SRN: PL-MF-000040289
Country: Poland
Email: medical.devices@rehabed.com.pl
Phone: 32 346 00 33

Variants by status