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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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Sacca non sterile per raccolta urina — 6 UDI-DI variants, MDR

MD Atlas
Chimed s.r.l.

Data from EUDAMED, last updated May 30, 2026

Sacca non sterile per raccolta urina

805896469UROBAG10X9G

6 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: Chimed s.r.l.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805896469UROBAG10X9G
Device name: Sacca non sterile per raccolta urina
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Chimed s.r.l.
SRN: IT-MF-000016095
Country: Italy
Email: info@chimed.it
Phone: +390586427333

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KM60QXC6BNE0D8EA8XETTYCG

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

10456108058964696403
10124408058964696380
10314408058964696618
10214008058964696465
10214408058964696106
10314808058964696625