Pro-Lab Diagnostics UK
United Kingdom (ex Northern Ireland) GB-MF-000003833 Last updated 23 May 2026
- Devices
- 274
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Factor i Ref PL.6133
Factor d Ref PL.6113
Group F Factor 11 Ref PL.6022
Group C2 Factor 8 Ref PL.6014
Factor h Ref PL.6118
Group I Factor 16 Ref PL.6029
Factor s Ref PL.6126
Factor b Ref PL.6111
Factor f Ref PL.6129
Factor enz15 Ref PL.6117
Group G1 Factor 22 Ref PL.6024
Immersion Oil Ref PL.396
Rabbit Coagulase Plasma 10.0 ml Ref PL.850-10
Factor m Ref PL.6127
Factor q Ref PL.6131
Group G Factor 13, 22, 23 Ref PL.6023
Polyvalent O A-I + Vi Ref PL.6000
Group M Factor 28 Ref PL.6033
Rapid Salmonella Diagnostics Sera RSD 3 Ref PL.6202
Inoclic Pack Ref PL.041003
G Complex Ref PL.6121
Factor a Ref PL.6110
Group E4 Factor 19 Ref PL.6020
Rapid Salmonella Diagnostics Sera RSD 2 Ref PL.6201
Showing 251-274 of 274
Related companies
Authorised representatives
What Pro-Lab Diagnostics UK makes
Pro-Lab Diagnostics UK manufactures laboratory reagents and stains for microbiological and histological testing, including concentrated and ready-to-use solutions like Auramine Phenol, Lugol’s Iodine, and Ziehl-Neelsen Carbol Fuchsin. Their portfolio also includes Gram stain differentiators, Potassium Permanganate, and Factor I reagents, designed for diagnostic use in clinical laboratories.
These products fall under Class A (general laboratory reagents) and IVD General (in vitro diagnostics) classifications, and they are registered in the EUDAMED database. The company operates from the United Kingdom.
Frequently asked questions
What types of medical devices does Pro-Lab Diagnostics UK manufacture?
Pro-Lab Diagnostics UK specialises in laboratory reagents and stains used primarily for microbiological and histological testing. Their products include ready-to-use and concentrated solutions like Auramine Phenol, Lugol’s Iodine, and Ziehl-Neelsen Carbol Fuchsin, as well as Gram stain differentiators and other diagnostic reagents. These are designed to support accurate identification and analysis in clinical laboratory settings.
Where is Pro-Lab Diagnostics UK based, and how does that affect its devices?
Pro-Lab Diagnostics UK is based in the United Kingdom, which means its devices are subject to EU regulatory frameworks if marketed within the European Economic Area. The company’s products are registered in the EUDAMED database, ensuring compliance with EU requirements for in vitro diagnostics and general laboratory reagents.
Which regulatory registries list Pro-Lab Diagnostics UK’s devices?
Pro-Lab Diagnostics UK’s devices are listed in the EUDAMED database, which is the official EU registry for medical devices. This registry tracks manufacturers, devices, and regulatory information to ensure transparency and compliance with EU medical device regulations.
How are Pro-Lab Diagnostics UK’s devices classified under EU regulations?
Pro-Lab Diagnostics UK’s products fall under Class A (general laboratory reagents) and IVD General (in vitro diagnostics) classifications. Class A applies to low-risk items like basic reagents, while IVD General covers diagnostic tests used in clinical settings. Classification determines regulatory requirements, with IVD General devices requiring conformity assessment procedures before market placement.
Information
- Country
- United Kingdom (ex Northern Ireland)
- Address
- 3, Bassendale Road, Bromborough, United Kingdom (ex Northern Ireland)
- Website
- www.pro-lab.co.uk
- [email protected]
- Phone
- +44 (0) 151 353 1613
- PRRC contact
- Mike Owen
- EUDAMED SRN
- GB-MF-000003833