Mediplus, Ltd.
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Mediplus, Ltd. is a medical device manufacturer, with 178 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I; EU Class IIb and IIa) as of 13 Nov 2026.
- Devices
- 178
Registry facts
- Registries
- FDA GUDID 132
- EUDAMED 102
- FDA 510(k) 4
- Device classes
- FDA Class II 103
- FDA Class I 33
- EU Class IIb 26
- EU Class IIa 16
- Top EMDN categories
- Sites and related companies
- Mediplus Ltd. United Kingdom
- Identifiers
- DUNS 228480810
What Mediplus, Ltd. makes
Mediplus, Ltd. manufactures urodynamic measurement systems for bladder function assessment, including pressure monitoring tubing sets and male urinary outflow analysis cuffs. Their portfolio also includes urological drainage solutions such as indwelling urethral drainage balloons and suprapubic drainage catheters, as well as urological irrigation systems. Additionally, they produce gastrointestinal motility manometric catheters for diagnostic motility testing and capnography oxygen masks for respiratory monitoring during medical procedures.
The company’s devices are classified under FDA categories, with most falling under Class I and some under Class II. Products are listed via 510(k) premarket notifications and the FDA’s Unique Device Identifier (UDI) system.
Catalogue
Search and filter all 178 devicesShowing 1-50 of 178
Company details
- DUNS number
- 228480810
- help@mediplus.co.uk
- Phone
- +4401494551200
Sites
- Mediplus Ltd. GBFEI 3011308139 42 devices
Frequently asked questions
How many devices does Mediplus, Ltd. have in the registry?
The registry currently lists 178 devices for Mediplus, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mediplus, Ltd.'s devices?
Among its 50 most recently registered devices, Mediplus, Ltd. has devices listed in EUDAMED (46 devices) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Mediplus, Ltd.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Mediplus, Ltd.'s devices are Class I, Class IIa, Class IIb and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mediplus, Ltd. in the registry?
The most recently registered devices listed for Mediplus, Ltd. include Chalfont: Double lumen extension set: 1 x anti-siphon, 1 x high-flow back check valve (13cm/5"), Silicone 2 Way Foley (open tip) Catheter, 18Fr. 10cc, Standard, 42cm, Quintuple lumen extension set: 4 x anti-siphon, 1 x high-flow back check valve (250cm/98") and S-Cath™ System - Silicone Suprapubic Foley (open tip) Catheter, With Introducer Set, 12Fr. 10cc, 42cm.