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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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GastroFinder® 2SMART — 1 UDI-DI variant, IVDR (PathoFinder B.V.)

MD Atlas
PathoFinder B.V.

Data from EUDAMED, last updated May 30, 2026

GastroFinder® 2SMART

87193271161PF5600-2SVQ

1 UDI-DI variant

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: PathoFinder B.V.

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Identity & classification

Basic UDI-DI: 87193271161PF5600-2SVQ
Device name: GastroFinder® 2SMART
Device model: PF5600-2S
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Feb 21, 2023

Manufacturer & authorised representative

Manufacturer

Name: PathoFinder B.V.
SRN: NL-MF-000002704
Country: Netherlands
Email: info@pathofinder.com
Phone: +31 (0)43 30 30 400

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01GSSPZVTPZ49XZXJE8VRK5645

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

GastroFinder® 2SMART08719327116104