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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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P1506/PCE/LENGA/IGN — 3 UDI-DI variants, MDR (Storello Ausili SRL)

MD Atlas
Storello Ausili SRL

Data from EUDAMED, last updated May 30, 2026

P1506/PCE/LENGA/IGN

805495381CONT_LETTOXJ

3 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: Storello Ausili SRL

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805495381CONT_LETTOXJ
Device name: —
Device model: P1506/PCE/LENGA/IGN
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 30, 2026

Manufacturer & authorised representative

Manufacturer

Name: Storello Ausili SRL
SRN: IT-MF-000045673
Country: Italy
Email: norman@storelloausili.com
Phone: +393405104886

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KQFG6GBB7S1CRX1H5K715134

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

P1505/PCE/LEN/IGN08054953810874
P1506/PCE/LENGA/IGN08054953810867
SACCONANNA08054953810881