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?

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

BI 220/A07640137453251
BA 205/A07640137453206
BA 200/A07640137453190
BI 223/A07640137453275
BI 240/A07640137453268
BA 214/A07640137453220
BA 219/A07640137453244
BA 218/A07640137453237
BI 229/A07640137453305
BA 213/A07640137453213
BA 261/A07640137453817
BI 228/A07640137453299
BI 224/A07640137453282
BA 260/A07640137453800
BA 100/T07640137450250
1901-532107640137454050
BA 113/T07640137453114
BI 140/T07640137450397
BA 118/T07640137453145
BA 114/T07640137453121
BIO 122/T07640137450410
BA 102/T07640137450267
BAO 102/T07640137450328
BI 128/T07640137453169
BA 119/T07640137453152

1 2 3 4

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