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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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Puffi OP swing/small edition — 2 UDI-DI variants, MDR

MD Atlas
Prova Nova GmbH

Data from EUDAMED, last updated May 23, 2026

Puffi OP swing/small edition

4250551600000024H

2 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: Prova Nova GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4250551600000024H
Device name: Puffi OP swing/small edition
Device model: OP Hocker + Rücken
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 2, 2024

Manufacturer & authorised representative

Manufacturer

Name: Prova Nova GmbH
SRN: DE-MF-000017745
Country: Germany
Email: info@provanova.de
Phone: +4923313754380

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01JBPM6BWHGW3523X8T1BWT9M8

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

3204/3205/3206/3207/3294/3295/3296/329704250551699161
3244/3245/3246/3247/3274/3275/3276/327704250551699178