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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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Nitzbon Helparm — 1 UDI-DI variant, MDD (Nitzbon AG)

MD Atlas
Nitzbon AG

Data from EUDAMED, last updated May 31, 2026

Nitzbon Helparm

B-04260101483027

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class I

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Manufacturer: Nitzbon AG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: B-04260101483027
Device name: Nitzbon Helparm
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class I
Version date: May 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: Nitzbon AG
SRN: DE-MF-000009971
Country: Germany
Email: jn@nitzbon.org

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSQQ96D4T3YEE5SPP4H83KRQ

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

Nitzbon Helparm04260101483027