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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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Bambi Interface — 1 UDI-DI variant, MDR (Bambi Belt B.V.)

MD Atlas
Bambi Belt B.V.

Data from EUDAMED, last updated May 30, 2026

Bambi Interface

8720256769BI014F

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Bambi Belt B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 8720256769BI014F
Device name: Bambi Interface
Device model: BI-N01
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Bambi Belt B.V.
SRN: NL-MF-000010914
Country: Netherlands
Email: info@bambi-medical.com
Phone: +31402881177

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KMG7HGC5C9A2JJSYR0RVV0H1

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

Bambi Interface87202567690055