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.

ANTEPARTUM/PRINTER — 91 UDI-DI variants, MDR (ArjoHuntleigh AB)

MD Atlas
ArjoHuntleigh AB

Data from EUDAMED, last updated May 30, 2026

ANTEPARTUM/PRINTER

5060693520389WY

91 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
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: 5060693520389WY
Device name: ANTEPARTUM/PRINTER
Device model: TEAM3A
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Nov 21, 2025

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

91 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

basicUdiUlid01KAKCENJ0C3NXQDBKA1YWAE5X

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

TEAM3A 305051968035196
TEAM3I NZB305051968047779
SC3SW/30BED05051968042880
SC3/CLIENTCNC05051968042767
TEAM3I05051968032584
TEAM3I M05051968042033
TEAM3I NZB05051968047861
SC3/HL7EXP05051968042798
TEAM3I NZ05051968047854
TEAM3A M305051968047229
SC3/PARTO05051968042811
TEAM3I NB305051968035325
TEAM3A MB305051968047236
SC3SYS/30BED05051968044556
SC3SYS/8BED05051968044525
TEAM3A B05051968032492

1 2 3 4