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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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PALMPRO EXPERT 631- Taglia Extra piccola — 37 UDI-DI variants, MDR

MD Atlas
ICOGUANTI S.p.A.

Data from EUDAMED, last updated May 30, 2026

PALMPRO EXPERT 631- Taglia Extra piccola

8005830GLPFYN

37 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: ICOGUANTI S.p.A.

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Device characteristics

Administers medicine

Identity & classification

Basic UDI-DI: 8005830GLPFYN
Device name: PALMPRO EXPERT 631- Taglia Extra piccola
Device model: Guanti monouso da esame in lattice naturale senza polvere
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2026

Manufacturer & authorised representative

Manufacturer

Name: ICOGUANTI S.p.A.
SRN: IT-MF-000053804
Country: Italy
Email: g.ageno@icoguanti.it
Phone: +39 010218298

Variants by status

UDI-DI variants

37 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRNZR3AJW9PEJB0BQ8JVRZTR

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

EHP/S08005830010665
EHP/L08005830010689
EHP/M08005830010672
EHRP/XL08005830008310
EHRP/XXL08005830009805
EHRP/L08005830008303
EHRP/M08005830008297
EHRP/S08005830008280
DTPF/S08005830011969
DTPF/XS08005830011952
DTPF/L08005830011983
DTPF/M08005830011976

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