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EUDAMED registration 08964004187025No

Nail Nipper Straight Cut

HAFEEZ IMPEX INTERNATIONALClass IEU EUDAMEDTrade name: HAFEEZ IMPEX INTERNATIONAL
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
L99
Trade name
HAFEEZ IMPEX INTERNATIONAL
Implantable
No
Reusable
Yes
Measuring function
No
Registration information
Primary DI
08964004187025
Basic UDI
8964004187NAILNIPPERSPG
Active status
No
Manufacturer
Country
Pakistan
Country type
NON_EU
Address
Hashim Pura, Defense Road, Sialkot
Email
info@hafeezimpex.com
Authorized representative
SRN
ES-AR-000000293
Country
Spain
Address
C/ Horacio Lengo N18 Málaga
Email
info@cmcmedicaldevices.com
Telephone
+34951214054
Regulatory information
Competent authority
Danish Medicines Agency, Pharmacovigilance & Medical Devices
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Austria
Market available
Austria:None~None, Belgium:None~None, Denmark:None~None, Finland:None~None, France:None~None, Germany:None~None, Hungary:None~None, Ireland:None~None, Italy:None~None, Netherlands:None~None, Norway:None~None, Sweden:None~None, Türkiye:None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

SURGICAL INSTRUMENTS, REUSABLE - OTHER

About this record

Access comprehensive regulatory information for Nail Nipper Straight Cut 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 08964004187025 and manufactured by HAFEEZ IMPEX INTERNATIONAL in Pakistan.

This page provides complete registration details including trade name (HAFEEZ IMPEX INTERNATIONAL), manufacturer information, authorized representative details, competent authority (Danish Medicines Agency, Pharmacovigilance & Medical Devices), 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.