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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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Elafast® — 1 UDI-DI variant, IVDR (Eurospital Spa)

MD Atlas
Eurospital Spa

Data from EUDAMED, last updated May 30, 2026

Elafast®

802816920BW01020608053R

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: Eurospital Spa

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Device characteristics

ReagentProfessional testingAnimal tissues / cells

Clinical investigations

Registered: No

Identity & classification

Basic UDI-DI: 802816920BW01020608053R
Device name: Elafast®
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Feb 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Eurospital Spa
SRN: IT-MF-000028468
Country: Italy
Email: regulatory@eurospital.it
Phone: +3904089971

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KJFKMZSJN3GGKG5V0K2XTQ2V

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

9191EP08028169208411