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EUDAMED registration 06222012099092No

Plaster Roll

Miracle Medical IndustriesClass IEU EUDAMEDTrade name: Miracle SILK PLASTER 5 CM
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
M050199
Trade name
Miracle SILK PLASTER 5 CM
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06222012099092
Basic UDI
6222012027491N6
Version date
September 12, 2024
Manufacturer last update
January 11, 2023
Active status
No
Manufacturer
Manufacturer name
Miracle Medical Industries
Country
Egypt
Country type
NON_EU
Address
El Obour City
Email
wael@Tatweer-eg.com
Authorized representative
Name
CMC Medical Devices & Drugs SL
SRN
ES-AR-000000293
Country
Spain
Address
C/ Horacio Lengo N18 Málaga
Email
info@cmcmedicaldevices.com
Telephone
+34951214054
Regulatory information
Competent authority
Agencia Española de Medicamentos y Productos Sanitarios
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Greece
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

SURGICAL PLASTERS - OTHER

About this record

Access comprehensive regulatory information for Plaster Roll 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 06222012099092 and manufactured by Miracle Medical Industries in Egypt.

This page provides complete registration details including trade name (Miracle SILK PLASTER 5 CM), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.