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.

ENTERPRISE 9000X — 514 UDI-DI variants, MDR (ArjoHuntleigh AB)

MD Atlas
ArjoHuntleigh AB

Data from EUDAMED, last updated May 30, 2026

ENTERPRISE 9000X

5060693520075W6

514 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: ArjoHuntleigh AB

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

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 5060693520075W6
Device name: ENTERPRISE 9000X
Device model: 9X21AE111BFCSA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 31, 2024

Manufacturer & authorised representative

Manufacturer

Name: ArjoHuntleigh AB
SRN: SE-MF-000000696
Country: Sweden
Email: info@arjo.com
Phone: +46 10 335 4500

Variants by status

UDI-DI variants

514 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

basicUdiUlid01HZ6R14R81Q9ZCS19KV8GQQT5

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

9X22BE011FCAAB05055982754194
9X22CR111FFACB05055982785761
9X21AN011FEABB05055982753555
9X21AB101BAAAA05059441101765
9X22BQ011BDABA05055982754538
9X22BY111FCBOA05056097366852
9X22BY111FFAZA05055982754897
9X22BF111BAACA05055982754293
9X21AQ101BFABA05055982753609
9X21AQ111BFBOA05056097335216
9X22BB101AAAAA05055982758222
9X21CH111DFCSA05055982753852
9X24BE101FCAAA05059441137375
9X22BZ111BFACA05055982754880
9X21AC101BBBOA05055982753388
9X21AE111BCABB05055982785679
9X22FD111BBAKA05055982753319
9X21EQ101BABOA05059441132462
9X21HQ111FFAIB05056097334288
9X22GN101BDABA05059441141587
9X22FC111BFAEA05059441100195
9X21AR111BFADA05055982753661
9X24BD101FAAAA05059441126225
9X21EQ131DBADA05059441137603
9X22BC101FBAAB05056097321486