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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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UNICO - PERCUTANEOUS KIT CH 9 — 28 UDI-DI variants, MDR (Redax S.p.A.)

MD Atlas
Redax S.p.A.

Data from EUDAMED, last updated May 31, 2026

UNICO - PERCUTANEOUS KIT CH 9

803413929UNICO1aRF

28 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Redax S.p.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 803413929UNICO1aRF
Device name: UNICO - PERCUTANEOUS KIT CH 9
Device model: 10800
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Apr 29, 2025

Manufacturer & authorised representative

Manufacturer

Name: Redax S.p.A.
SRN: IT-MF-000019320
Country: Italy
Email: gianluca.boni@redax.it

Variants by status

UDI-DI variants

28 UDI-DI variants

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Applied filters

basicUdiUlid01JT0ENSFG4CYVSMPW17C4TW1R

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

No registered UDI-DI variants for this device family.