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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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STD-Finder® 2SMART — 1 UDI-DI variant, IVDD (PathoFinder B.V.)

MD Atlas
PathoFinder B.V.

Data from EUDAMED, last updated May 30, 2026

STD-Finder® 2SMART

B-08719327116128

1 UDI-DI variant

IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]IVDD — Annex II List B

Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List B
Manufacturer: PathoFinder B.V.

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Legacy certificates

Certificate number: CE 737648
Type: refdata.legacy.ivdd-certificate-type.iv-excluding-4-6
Notified body: BSI Group The Netherlands B.V. (2797)
Validity: May 1, 2024

Identity & classification

Basic UDI-DI: B-08719327116128
Device name: STD-Finder® 2SMART
Device model: PF3200-2S
Issuing agency: EUDAMED
Legislation: IVDD [Directive 98/79/EC on in vitro diagnostic medical devices]
Risk class: IVDD — Annex II List B
Version date: Jun 14, 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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Export results

Applied filters

basicUdiUlid01H2X2G7VGHM61C2P9TH2BT9AZ

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

STD-Finder® 2SMART08719327116128