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Manufacturer profile

Abbott Ireland Diagnostics Division, Finisklin Business Park, Sligo, Ireland

Albania25 devices registered in Albania1 risk classNov 21, 2019 – Sep 08, 2022
VerifiedAKBPM · official registry
25
Total devices
1
Risk classes
2019
Earliest registration
2022
Latest registration
Regulatory footprint
Search Abbott Ireland Diagnostics Division, Finisklin Business Park, Sligo, Ireland across other regulatory registries
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Recent registrations
Latest 10 Albania device registrations
Alinity i HBsAg Reagent Kit: 08P0822, 08P0832, 08P0852, 08P0857; Alinity HBsAg Calibrators: 08P0801; Alinity i HBsAg Controls: 08P0810
12737
Invitro · Sep 08, 2022
ARCHITECT CEA Reagent Kit
11028
Invitro · Jan 10, 2022
ARCHITECT Free PSA Reagent Kit
11026
Invitro · Jan 10, 2022
ARCHITECT Free PSA
10511
Invitro · Nov 03, 2021
Architect Anti-HBs Reagent Kit
10313
Invitro · Oct 15, 2021
Architect HBsAG Reagent kit
10309
Invitro · Oct 15, 2021
ARCHITECT Rubella IgM Reagent Kit: 6C18-25 (100 tests); ARCHITECT Rubella IgM Calibrator: 6C18-01; ARCHITECT Rubella IgM Controls: 6C18-10
10303
Invitro · Oct 14, 2021
HbsAg Qualitative Confirmatory Manual Diluent
9994
Invitro · Aug 16, 2021
Alinity i Rubella IgM Reagent Kit; Calibrators; Controls
8208
Invitro · Oct 07, 2020
Alinity i AFP reagent Kit; Calibrator'; Control
8190
Invitro · Oct 06, 2020
View all 25 devices →
Risk class distribution
Devices by risk class
Invitro25100.0% of total
About this profile

Explore comprehensive manufacturer profile for Abbott Ireland Diagnostics Division, Finisklin Business Park, Sligo, Ireland through Pure Global AI's free Albania medical device database. This company manufactures 25 medical devices registered in Albania across 1 risk class. Their registration history spans from Nov 21, 2019 to Sep 08, 2022.

This page provides detailed insights including recent registrations, risk class distribution (Invitro: 25), and complete regulatory information from the official Albania medical device database. Pure Global AI offers free access to Albania's complete medical device registry.