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Manufacturer profile

Penlon Limited

EU EUDAMEDUnited Kingdom (ex Northern Ireland)42 registered devices
VerifiedEUDAMED · official EU database
42
Total devices
2
Risk classes
2025
Earliest version
2025
Latest version
Regulatory footprint
Search Penlon Limited across other regulatory registries
ThailandColombiaSouth KoreaCanadaEcuadorSaudi Arabia
Recent products (latest 10)
Most recently updated devices in the database
Diamond Fibrelight Handle
05051977001892
Class I
Diamond S
05051977001304
Class I
Diamond Fibrelight Handle
05051977001908
Class I
Diamond Fibrelight Handle
05051977001915
Class I
Diamond S
05051977001328
Class I
Laryngoscope blade, reusable
05051977001731
Class I
Laryngoscope blade, reusable
05051977001601
Class I
Laryngoscope blade, reusable
05051977001724
Class I
Laryngoscope blade, reusable
05051977001700
Class I
Laryngoscope blade, reusable
05051977001694
Class I
Risk class distribution
Breakdown by risk classification
Class I3992.9% of total
Class IIb37.1% of total
Top authorized representatives
Most common authorized representatives for this manufacturer
Obelis s.a.
100.0%42 devices
About this profile

Explore comprehensive manufacturer profile for Penlon Limited through Pure Global AI's free EU medical device database. This company manufactures 42 medical devices registered with EUDAMED across 2 risk classes based in United Kingdom (ex Northern Ireland).

This page provides detailed insights including recent registrations, risk class distribution (Class I: 39, Class IIb: 3), and complete regulatory information from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry.