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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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OBF - Oral BioFilter — 2 UDI-DI variants, MDR (FAMADENT, S.L.U.)

MD Atlas
FAMADENT, S.L.U.

Data from EUDAMED, last updated May 23, 2026

OBF - Oral BioFilter

84354577-00024W

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: FAMADENT, S.L.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84354577-00024W
Device name: OBF - Oral BioFilter
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 27, 2021

Manufacturer & authorised representative

Manufacturer

Name: FAMADENT, S.L.U.
SRN: ES-MF-000000270
Country: Spain
Email: protechno@protechno.com
Phone: +34 972526169

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01FJ1FYJBRCQA2GWWKH72DW8FR

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

OBF - Box 40 UN08435457718154
OBF-00608435457718147