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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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Pads — 8 UDI-DI variants, IVDR (Copan Wasp S.r.l.)

MD Atlas
Copan Wasp S.r.l.

Data from EUDAMED, last updated May 30, 2026

Pads

805014821IP170APADSM06TJ

8 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Copan Wasp S.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805014821IP170APADSM06TJ
Device name: Pads
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Feb 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: Copan Wasp S.r.l.
SRN: IT-MF-000012489
Country: Italy
Email: regulatory.wasp@copangroup.com
Phone: +393316746551

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FVA5716FC3TFAFWJXEV23MYK

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

WR086-03-000318050148210129
WR086-03-001018050148210600
WR093-01-000418052870817676
WR086-61-001418050148210105
WR086-03-000118050148210112
WR086-50-000118050148210181
WR086-03-000418050148210136
WR091-11-000118050148212857