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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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DFB850 — 4 UDI-DI variants, IVDR (Gruppo Strola srl)

MD Atlas
Gruppo Strola srl

Data from EUDAMED, last updated May 31, 2026

DFB850

805663343C0001VV

4 UDI-DI variants

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

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Gruppo Strola srl

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805663343C0001VV
Device name: DFB850
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Gruppo Strola srl
SRN: IT-MF-000054807
Country: Italy
Email: info@gruppostrola.com
Phone: +390117390860

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01KSHRWBEVNFPEVF1TPQNMB7MG

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

DFB850-F-B80566334305564
DFB850-F-S80566334305328
DFB850-X-S80566334305496
DFB850-X-B80566334305632