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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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Specimen collection cup — 2 UDI-DI variants, IVDR

MD Atlas
Edif Instruments S.r.l.

Data from EUDAMED, last updated May 30, 2026

Specimen collection cup

805360894CML00716G8

2 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: Edif Instruments S.r.l.

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Device characteristics

Professional testing

Identity & classification

Basic UDI-DI: 805360894CML00716G8
Device name: —
Device model: Specimen collection cup
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 31, 2022

Manufacturer & authorised representative

Manufacturer

Name: Edif Instruments S.r.l.
SRN: IT-MF-000009556
Country: Italy
Email: info@edif.it

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G4DB354PSPW4FG66DYF4ENN8

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

Pack of specimen collection cups (1000 pc)80536089405222
Specimen collection micro-tube, 0,75 mL80536089405154