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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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GAF® FIXATIVE — 13 UDI-DI variants, IVDR (ADDAX BIOSCIENCES S.R.L.)

MD Atlas
ADDAX BIOSCIENCES S.R.L.

Data from EUDAMED, last updated May 31, 2026

GAF® FIXATIVE

805797751GAF001CS

13 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: ADDAX BIOSCIENCES S.R.L.

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Device characteristics

Reagent

Identity & classification

Basic UDI-DI: 805797751GAF001CS
Device name: GAF® FIXATIVE
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Jan 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: ADDAX BIOSCIENCES S.R.L.
SRN: IT-MF-000028891
Country: Italy
Email: administration@addaxbio.com
Phone: 3887798977

Variants by status

UDI-DI variants

13 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KFMZ51MWQ0EQE8JZMY918SWA

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

GAF001000B108057977510072
GAF010000B108057977510102
GAF000010P4008057977510003
GAF000125P2408057977510041
GAF000025P4008057977510010
GAF000250B808057977510065
GAF000250P1208057977510058
GAF003000P108057977510126
GAF003000B108057977510089
GAF005000B108057977510096
GAF000090P2408057977510034
GAF000090P1208057977510027
GAF001000P108057977510119