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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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Autostoelen — 3 UDI-DI variants, MDR (Peereboom BV)

MD Atlas
Peereboom BV

Data from EUDAMED, last updated May 30, 2026

Autostoelen

87202995789autostoel-058U

3 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: Peereboom BV

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87202995789autostoel-058U
Device name: Autostoelen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 3, 2024

Manufacturer & authorised representative

Manufacturer

Name: Peereboom BV
SRN: NL-MF-000006609
Country: Netherlands
Email: info@peereboom.com
Phone: +31 (0)23 561 73 19

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01J6VDPD1Y56VMYDC5CNX4WXSE

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

Stingray i-Light autostoel08719327551875
Stingray i-Light Swing-out autostoel08719327551882
Stingray Swing-out autostoel08719327551868