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EUDAMED registration 05051977001700No

Laryngoscope blade, reusable

Penlon LimitedClass IEU EUDAMEDTrade name: Diamond Fibrelight Miller / Laryngoscope Blade Size 3
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
Z12021003
Trade name
Diamond Fibrelight Miller / Laryngoscope Blade Size 3
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
05051977001700
Basic UDI
5051977LAR-RUBLXV
Version date
February 26, 2025
Manufacturer last update
June 16, 2022
Active status
No
Manufacturer
Manufacturer name
Penlon Limited
Country
United Kingdom (ex Northern Ireland)
Country type
NON_EU
Address
Penlon, Barton Lane Abingdon
Email
techsupport@penlon.com
Authorized representative
Name
Obelis s.a.
SRN
BE-AR-000000106
Country
Belgium
Address
53 Boulevard Général Wahis Brussels
Email
regulatory@obelis.net
Telephone
+32(2)73 25 954
Regulatory information
Competent authority
Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Latvia
Market available
Hungary:None~None, Latvia:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

LARYNGOSCOPES

About this record

Access comprehensive regulatory information for Laryngoscope blade, reusable in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05051977001700 and manufactured by Penlon Limited in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Diamond Fibrelight Miller / Laryngoscope Blade Size 3), manufacturer information, authorized representative details, competent authority (Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten/ Afdeling Gezondheidsproducten), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.