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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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GUANTI IN LATTICE MONOUSO — 5 UDI-DI variants, MDR (Copag S.p.a.)

MD Atlas
Copag S.p.a.

Data from EUDAMED, last updated May 30, 2026

GUANTI IN LATTICE MONOUSO

8059028TOPT010201UV

5 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: Copag S.p.a.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8059028TOPT010201UV
Device name: GUANTI IN LATTICE MONOUSO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Copag S.p.a.
SRN: IT-MF-000015995
Country: Italy
Email: info@copag.it
Phone: +39 0636737200

Variants by status

UDI-DI variants

5 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSMAK9ZH0FSAD3KCKGY1Q80Y

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

1844108059028184416
1844208059028184423
2732008059028273202
3660008059028366003
1844308059028184430