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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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PENELOPE MANUAL DOSING EMERGENCY KIT — 1 UDI-DI variant, MDR

MD Atlas
SOL GROUP LAB S.r.l.

Data from EUDAMED, last updated May 31, 2026

PENELOPE MANUAL DOSING EMERGENCY KIT

805571326EMERGKITPG6

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SOL GROUP LAB S.r.l.

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 805571326EMERGKITPG6
Device name: PENELOPE MANUAL DOSING EMERGENCY KIT
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Aug 28, 2025

Manufacturer & authorised representative

Manufacturer

Name: SOL GROUP LAB S.r.l.
SRN: IT-MF-000025276
Country: Italy
Email: info@solgrouplab.it
Phone: +39 0444 290411

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01K3QZ33RQ10TG0GXKC4KSHMJP

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

PENELOPE MANUAL DOSING EMERGENCY KIT08055713260281