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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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Loophulpen — 5 UDI-DI variants, MDR (Peereboom BV)

MD Atlas
Peereboom BV

Data from EUDAMED, last updated May 30, 2026

Loophulpen

87202995789loophulp-03UQ

5 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: 87202995789loophulp-03UQ
Device name: Loophulpen
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Aug 27, 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

5 UDI-DI variants

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Applied filters

basicUdiUlid01J69JR8K9AG0R0CA3F0TDG5X1

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

Caddy loophulp FT08719327551813
Caddy loophulp Evo08720299578999
Janneke loophulp Evo08720299578982
Janneke loophulp FT08719327551806
Jasmijn loophulp Combi08719327551820