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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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AVIZOR HERBAL ALL IN ONE PE — 2 UDI-DI variants, MDR (AVIZOR S.A.)

MD Atlas
AVIZOR S.A.

Data from EUDAMED, last updated May 23, 2026

AVIZOR HERBAL ALL IN ONE PE

8431306104AVHERBALAIOPEPE

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: AVIZOR S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431306104AVHERBALAIOPEPE
Device name: AVIZOR HERBAL ALL IN ONE PE
Device model: AV-TF-104
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Dec 10, 2025

Manufacturer & authorised representative

Manufacturer

Name: AVIZOR S.A.
SRN: ES-MF-000020208
Country: Spain
Email: regulatory@avizor.es
Phone: +34 916564515

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01KC3TSW2Z49KZAEXDX6GRD2HQ

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

PT8806M08431306077625
PT8807M08431306088072