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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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Probetection — 42 UDI-DI variants, MDR (Palmedic)

MD Atlas
Palmedic

Data from EUDAMED, last updated May 30, 2026

Probetection

871737174PROBETECT-IIa-7P

42 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Palmedic

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871737174PROBETECT-IIa-7P
Device name: Probetection
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 6, 2026

Manufacturer & authorised representative

Manufacturer

Name: Palmedic
SRN: NL-MF-000007850
Country: Netherlands
Email: info@palmedic.eu
Phone: +31544370900

Variants by status

UDI-DI variants

42 UDI-DI variants

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Applied filters

basicUdiUlid01KGS4SVPGH582E5Q6M3MS6MMZ

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

No registered UDI-DI variants for this device family.