Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Instrumente Ir Raspeladapter Metall — 13 UDI-DI variants, MDR

MD Atlas
Falcon Medical Medizinische Spezialprodukte GmbH

Data from EUDAMED, last updated May 31, 2026

Instrumente Ir Raspeladapter Metall

9010018-01-01-001000004H

13 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

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

Reusable

Identity & classification

Basic UDI-DI: 9010018-01-01-001000004H
Device name: —
Device model: Instrumente Ir Raspeladapter Metall
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

13 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSAA0MYW8SFV38VS84MX3Z5Y

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

10-1090-10709010098001101
10-1090-10309010098001064
10-1090-10209010098001057
10-1090-16009010098007691
10-1090-15909010098007684
10-1090-14809010098001194
10-1090-15509010098001200
10-1090-14509010098001163
10-1090-15609010098006038
10-1090-15809010098007189
10-1090-15709010098007172
10-1090-14709010098001187
10-1090-14609010098001170