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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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ibesan MAX — 1 UDI-DI variant, MDR (Natur Produkt Zdrovit Sp. z o.o.)

MD Atlas
Natur Produkt Zdrovit Sp. z o.o.

Data from EUDAMED, last updated May 31, 2026

ibesan MAX

5904730876MD_NPZ_0217W

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Natur Produkt Zdrovit Sp. z o.o.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: TNP/MDR/0048/5905/2026
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: TUV NORD Polska Sp. z o.o (2274)
Validity: Feb 13, 2026 → Feb 12, 2029

Identity & classification

Basic UDI-DI: 5904730876MD_NPZ_0217W
Device name: ibesan MAX
Device model: Zawiesina w saszetkach
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Feb 16, 2026

Manufacturer & authorised representative

Manufacturer

Name: Natur Produkt Zdrovit Sp. z o.o.
SRN: PL-MF-000010540
Country: Poland
Email: naturprodukt@naturprodukt.pl

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KHKA6XZBED05QZDNV9HW3MQN

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

010-IBMAXZ05906204023935