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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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Rubber foam profile fi 5mm — 2 UDI-DI variants, MDR (Pamel d.o.o.)

MD Atlas
Pamel d.o.o.

Data from EUDAMED, last updated May 24, 2026

Rubber foam profile fi 5mm

385889415EEGACCESSORIESHN

2 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: Pamel d.o.o.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 385889415EEGACCESSORIESHN
Device name: Rubber foam profile fi 5mm
Device model: SR
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: Pamel d.o.o.
SRN: HR-MF-000028336
Country: Croatia
Email: pamel@pamel.hr
Phone: ++ 385 1 3473 134

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GKNY29CG9CTGJ21VPZWBAEQ9

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

Rubber foam profile fi 5mm03858894154357
Sponge holder CEC03858894153619