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.

Invasive Blood Pressure Trunk Cables — 17 UDI-DI variants, MDR

MD Atlas
GE Healthcare Finland Oy

Data from EUDAMED, last updated May 23, 2026

Invasive Blood Pressure Trunk Cables

8406821BUG00043GW

17 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: GE Healthcare Finland Oy

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 device

Identity & classification

Basic UDI-DI: 8406821BUG00043GW
Device name: Invasive Blood Pressure Trunk Cables
Device model: 2103966-001
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Dec 21, 2021

Manufacturer & authorised representative

Manufacturer

Name: GE Healthcare Finland Oy
SRN: FI-MF-000001176
Country: Finland
Email: eudamed@gehealthcare.com

Variants by status

UDI-DI variants

17 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

basicUdiUlid01FNE3KQNZZ89387MPRRYP4950

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

2104162-00200840682136549
2104162-00300840682136327
2104166-00200840682136358
2104162-00400840682136525
2104158-00200840682136556
2103966-00100840682136341
2104107-00400840682136464
2104158-00400840682136501
2104166-00300840682136396
2104158-00100840682136518
2104166-00100840682136488
2104158-00300840682136334
2104166-00400840682136570
2104162-00100840682136457
2104107-00100840682136563
2104107-00200840682136365
2104107-00300840682136587