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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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SPOON PS 2,5; 3,75 and 5ml, PANDA print — 2 UDI-DI variants, MDR

MD Atlas
TEHNOPRO d.o.o.

Data from EUDAMED, last updated May 24, 2026

SPOON PS 2,5; 3,75 and 5ml, PANDA print

385888353SpoonPandaFrogTT

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: TEHNOPRO d.o.o.

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 385888353SpoonPandaFrogTT
Device name: SPOON PS 2,5; 3,75 and 5ml, PANDA print
Device model: SPOON PS ,PANDA print
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 8, 2023

Manufacturer & authorised representative

Manufacturer

Name: TEHNOPRO d.o.o.
SRN: HR-MF-000025711
Country: Croatia
Email: tehnopro@tehnopro.hr
Phone: +38512409170

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01GV122KXPX8H19HHJNQM9RPVN

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

SPOON PS 2,5; 3,75 and 5ml,CE, PANDA PRINT03858883539554
SPOON PS 2,5; 3,75 and 5ml, CE, FROG PRINT03858883539592