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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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Stretcher — 16 UDI-DI variants, MDR (FAZZINI SRL)

MD Atlas
FAZZINI SRL

Data from EUDAMED, last updated May 31, 2026

Stretcher

805188799DT004E7

16 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: FAZZINI SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805188799DT004E7
Device name: Stretcher
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 9, 2026

Manufacturer & authorised representative

Manufacturer

Name: FAZZINI SRL
SRN: IT-MF-000035989
Country: Italy
Email: INFO@FAZZINI.IT
Phone: +39 022651521

Variants by status

UDI-DI variants

16 UDI-DI variants

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Applied filters

basicUdiUlid01KNRWXT3K8Z1CNKM43Y1TMEZV

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

Stretcher08051887991105
Stretcher08051887991150
Stretcher08051887991051
Stretcher08051887991075
Stretcher08051887991099
Stretcher08051887991082
Stretcher08051887996599
Stretcher08051887994731
Stretcher08051887991068
Stretcher08051887991143
Stretcher08051887994717
Stretcher08051887994700
Stretcher08051887994724
Stretcher08051887994748
Stretcher08051887991112
Stretcher08051887991136