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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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duoSHIELD™ PFT Latex 240 — 5 UDI-DI variants, MDR

MD Atlas
SHIELD Scientific B.V.

Data from EUDAMED, last updated May 30, 2026

duoSHIELD™ PFT Latex 240

87196320765412XW4

5 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: SHIELD Scientific B.V.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 87196320765412XW4
Device name: duoSHIELD™ PFT Latex 240
Device model: duoSHIELD™ PFT Latex 240
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 26, 2025

Manufacturer & authorised representative

Manufacturer

Name: SHIELD Scientific B.V.
SRN: NL-MF-000001691
Country: Netherlands
Email: info@shieldscientific.com
Phone: +31 (0)317 700 202

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KDCQE8TM9MT04A0JRFZKFY87

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

duoSHIELD™ PFT Latex 240 L08719632072478
duoSHIELD™ PFT Latex 240 M08719632072461
duoSHIELD™ PFT Latex 240 S08719632072454
duoSHIELD™ PFT Latex 240 XL08719632072485
duoSHIELD™ PFT Latex 240 XS08719632072447