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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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Inpoint Duo — 51 UDI-DI variants, MDR (INPOINT MEDICARE)

MD Atlas
INPOINT MEDICARE

Data from EUDAMED, last updated May 30, 2026

Inpoint Duo

5944759066ambsterilizA7

51 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: INPOINT MEDICARE

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Device characteristics

Measuring function

Identity & classification

Basic UDI-DI: 5944759066ambsterilizA7
Device name: Inpoint Duo
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 28, 2024

Manufacturer & authorised representative

Manufacturer

Name: INPOINT MEDICARE
SRN: RO-MF-000022427
Country: Romania
Email: office@inpointmedicare.com
Phone: +40743145407

Variants by status

UDI-DI variants

51 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JB97KZ1B6DPY5BQ42EPA6AD7

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

Sterilization reels with internal/external STEAM/ETO integrator type 5 , 75mmx200m05944759066243

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