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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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Instrumente I HXPE Presse Metall -… — 10 UDI-DI variants, MDR

MD Atlas
Falcon Medical Medizinische Spezialprodukte GmbH

Data from EUDAMED, last updated May 31, 2026

Instrumente I HXPE Presse Metall - Kunststoff

9010002-01-02-00000000R5

10 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: Falcon Medical Medizinische Spezialprodukte GmbH

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Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 9010002-01-02-00000000R5
Device name: —
Device model: Instrumente I HXPE Presse Metall - Kunststoff
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: Falcon Medical Medizinische Spezialprodukte GmbH
SRN: AT-MF-000001607
Country: Austria
Email: office@falcon-med.com
Phone: +43 2236 46465

Variants by status

UDI-DI variants

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSA82YMQAQYA4Q2ZEJC8TYS2

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

11-0092-05409010098008155
11-0092-05509010098008148
11-0092-13709010098003570
11-0092-13809010098003587
11-0092-13909010098003594
11-0092-14009010098003600
11-0092-14209010098003624
11-0092-05309010098008162
11-0092-13609010098003563
11-0092-14109010098003617