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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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IM-1090 TUBEGUARD — 1 UDI-DI variant, MDD (INORIS MEDICAL SP. Z O.O.)

MD Atlas
INORIS MEDICAL SP. Z O.O.

Data from EUDAMED, last updated May 30, 2026

IM-1090 TUBEGUARD

B-05902596226749

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: INORIS MEDICAL SP. Z O.O.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-05902596226749
Device name: IM-1090 TUBEGUARD
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: Oct 7, 2022

Manufacturer & authorised representative

Manufacturer

Name: INORIS MEDICAL SP. Z O.O.
SRN: PL-MF-000016864
Country: Poland
Email: j.lenart@inoris.pl
Phone: +48 663 977 556

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01GES02RD0J09K3VMK11V3T812

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

IM-1090 TUBEGUARD05902596226749