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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Braun ExactFit 1E / Braun ExactFit 2 — 5 UDI-DI variants, MDR

MD Atlas
KAZ Europe Sàrl

Data from EUDAMED, last updated May 23, 2026

Braun ExactFit 1E / Braun ExactFit 2

76307593BP4000CJ

5 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: KAZ Europe Sàrl

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 76307593BP4000CJ
Device name: Braun ExactFit 1E / Braun ExactFit 2
Device model: BUA4000 / BUA4050
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Dec 1, 2025

Manufacturer & authorised representative

Manufacturer

Name: KAZ Europe Sàrl
SRN: CH-MF-000029980
Country: Switzerland
Email: Quality_EMEA@helenoftroy.com

Authorised representative

Name: Obelis s.a.
SRN: BE-AR-000000106
Country: Belgium
Phone: +32(2)73 25 954

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KAB4590XDFAVJ3V1GD5PE97Q

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

Braun ExactFit 1, BUA4000EU07630759300095
Braun ExactFit 1, BUA4000EU07630759301900
Braun ExactFit 2, BUA4050EU07630759300125
Braun ExactFit 2, BUA4050EU07630759301931
Braun ExactFit 2, BUA4050EUAM07630759300156