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

9X22BQ101BDABA05055982754545
9X22CY101FDABA05056097300023
9X21AJ001DAABA05055982753470
9X22BJ111FCBOA05056097337777
9X22CQ111BFABA05056097301761
9X22CQ111DCCSA05055982754941
9X22BQ111BDBOA05055982754590
9X22BE101BDAKB05059441129769
9X21AR111BEADA05055982753647
9X21AL001BCBOA05059441134367
9X21AB101AAAAA05055982758161
9X21CR111FFAZA05056097362144
9X22BE111BDBNA05055982754248
9X22BF111BCACA05055982754330
9X21AA001ACABA05055982758130
9X22CL111BFCSA05056097320052
9X22FQ111DBADA05059441129974
9X22BH111DEADA05055982754439
9X21AB101FAAAA05055982753333
9X22BF111BBCSA05055982754323
9X21DL101FCCTB05059441021049
9X21DL001FFANA05056097356372
9X28G4111FFAJC05059441127147
9X22CD111BCAAB05056097359267
9X21AL001BABOA05059441134152