Pure Global

DL2 Battery - EUDAMED Registration 08559970069446

Access comprehensive regulatory information for DL2 Battery 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 08559970069446 and manufactured by DermLite LLC in United States.

This page provides complete registration details including trade name (DERMLITE), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), 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.

Free Database
Powered by Pure Global AI
EUDAMED Official Data
Class I
08559970069446
No
DL2 Battery
Trade Name: DERMLITE
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Description (EMDN)

DERMATOSCOPES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Z12040108
Trade Name
DERMLITE
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
08559970069446
Basic UDI
08559970069448L
Version Date
August 26, 2024
Manufacturer Last Update
June 09, 2023
Active Status
No
Manufacturer
Manufacturer Name
DermLite LLC
Country
United States
Country Type
NON_EU
Address
21 Argonaut Aliso Viejo CA
Email
info@ecrep.ie
Authorized Representative
SRN
IE-AR-000003995
Country
Ireland
Address
5 Fitzwilliam Square East Dublin D2
Email
info@ecrep.ie
Telephone
+353 89 225 1951
Regulatory Information
Competent Authority
Health Products Regulatory Authority, Medical Devices Department
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No