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

9X21DJ111FBBVB05055982753944
9X21EQ131DEADA05059441141440
9X21AR111BEBNB05055982753654
9X22BR111FEADA05055982754750
9X22BQ111BFABA05055982754606
9X21AQ101BEABA05055982753593
9X21DN001BBBOA05055982753951
9X21AR111FEBNB05055982753722
9X21AR111BBBNB05055982753623
9X21AE111BFCSA05055982753449
9X22BQ111FEABB05055982754651
9X21AJ101BBADB05055982753494
9X21AB101BAAAB05056341600725
9X21AQ101BDABA05055982753586
9X21AE001FBAAB05055982753418
9X22BQ011BABOA05056097336701
9X22CL131BFADB05059441129721
9X22BL101BFABA05055982754477
9X21AQ101AFAJA05055982758185
9X21CH111FEAAB05056097304113
9X21AJ101BEABB05056097341019
9X21DL111BBHRA05056341697534
9X22BR111FFADA05055982754767
9X21AJ021BBABA05056341601890
9X22BQ121BDABA05059441143383