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.

I/A System reusable — 78 UDI-DI variants, MDR (Bürki inno med AG)

MD Atlas
Bürki inno med AG

Data from EUDAMED, last updated May 23, 2026

I/A System reusable

764013745P02P04X4

78 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: Bürki inno med AG

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

Reusable

Identity & classification

Basic UDI-DI: 764013745P02P04X4
Device name: I/A System reusable
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Bürki inno med AG
SRN: CH-MF-000017443
Country: Switzerland
Email: info@buerki.eu
Phone: +41 71 744 88 66

Authorised representative

Name: Bürki inno med GmbH
SRN: DE-AR-000008073
Country: Germany

Variants by status

UDI-DI variants

78 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

basicUdiUlid01KPZSDW4WE6KNKS2Q54FP0MB9

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

BIO 120/T07640137450403
1901-552307640137454074
BAO 100/T07640137450311
BIO 128/T07640137451493
1901-542107640137454067
BI 126/T07640137450373
BA 107/T07640137451134
1901-592107640137454104
BA 108/T07640137450298
BI 121/T07640137450359
1901-582107640137454098
BI 129/T07640137453176
BI 125/T07640137450366
BI 123/T07640137453008
BIO 127/T07640137450427
BAO 110/T07640137451486
BAO 105/T07640137450335
BA 105/T07640137450281
BA 104/T07640137450274
BI 120/T07640137450342
1901-562307640137454081
BI 124/T07640137453138
SL 13007640137450687
1901-502107640137454029
SL 116 s107640137451790

1 2 3 4