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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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SMOKE EVACUATOR ARIA — 1 UDI-DI variant, MDR (EMED SP. Z O. O. SP. K.)

MD Atlas
EMED SP. Z O. O. SP. K.

Data from EUDAMED, last updated May 31, 2026

SMOKE EVACUATOR ARIA

59077632-TF7ARIA-W4

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: EMED SP. Z O. O. SP. K.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 59077632-TF7ARIA-W4
Device name: SMOKE EVACUATOR ARIA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: EMED SP. Z O. O. SP. K.
SRN: PL-MF-000012648
Country: Poland
Email: emed@emed.pl
Phone: + 48 22 723 08 00

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KS28BPC29SD23YQQ96WGQ0MW

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

Smoke evacuator ARIA05907763200195