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.

Electrical Reusable Equipment -… — 116 UDI-DI variants, MDR

MD Atlas
CODAN pvb Critical Care GmbH

Data from EUDAMED, last updated May 31, 2026

Electrical Reusable Equipment - Xtrans®/DPT-9000

4046765CABCBOKL

116 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: CODAN pvb Critical Care 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

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4046765CABCBOKL
Device name: Electrical Reusable Equipment - Xtrans®/DPT-9000
Device model: Zubehör / Accessory IBPM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: CODAN pvb Critical Care GmbH
SRN: DE-MF-000007510
Country: Germany
Email: stk@codanpvbcc.de
Phone: +49 (0) 8121 98020

Variants by status

UDI-DI variants

116 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

basicUdiUlid01KSKXC7G3XCE9GG5JZ3NXW8CJ

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

Monitor-Connector+, 3-fold - Standard04046765440060
Monitor-Connector+, 3-fold - Standard04046765435813
Monitor-Connector+, 3-fold - Standard04046765439958
Monitor-Connector+, 3-fold - Standard04046765440374
Monitor-Connector+, 3-fold - Standard04046765435837
Monitor-Connector+, 3-fold - Standard04046765440312
Monitor-Connector+, 3-fold - Standard04046765440107
Monitor-Connector+, 3-fold - Standard04046765439941
Monitor-Connector+, 3-fold - Standard04046765435752
Monitor-Connector+, 4-fold - Standard04046765435783
Monitor-Connector+, 4-fold - Standard04046765435738
Monitor-Connector+, 4-fold - Standard04046765439996
Monitor-Connector+, 4-fold - Standard04046765435844
Monitor-Connector+, 4-fold - Standard04046765440329
Monitor-Connector+, 4-fold - Standard04046765439989
Monitor-Connector+, 4-fold - Standard04046765440022

1 2 3 4 5