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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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Co Fix — 8 UDI-DI variants, MDR (Pikdare S.p.A.)

MD Atlas
Pikdare S.p.A.

Data from EUDAMED, last updated May 30, 2026

Co Fix

805809022920100J3

8 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: Pikdare S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805809022920100J3
Device name: Co Fix
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Pikdare S.p.A.
SRN: IT-MF-000010069
Country: Italy
Email: istituzionale@pec.pikdare.it
Phone: +39031729111

Variants by status

UDI-DI variants

8 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KKKVS98ZA0QPQJSAVF4ZQ560

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

5802292010000008058090046394
5802292010010008058090047605
5802292210010008058090047612
5802292310000008058090046424
5802292210000008058090046417
5802292110000008058090046400
5802292110010008058090047629
5802292310010008058090047636