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Disposable Flush Tip Nerve Stimulator Probe - EUDAMED Registration 16955739030310

Access comprehensive regulatory information for Disposable Flush Tip Nerve Stimulator Probe in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 16955739030310 and manufactured by Xi'an Friendship Medical Electronics Co., Ltd. in China.

This page provides complete registration details including trade name (Friendship Medical), 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.

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EUDAMED Official Data
Class IIa
16955739030310
No
Disposable Flush Tip Nerve Stimulator Probe
Trade Name: Friendship Medical
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Device Description (EMDN)

NERVOUS SYSTEM MONITORING SYSTEMS

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
Z121002
Trade Name
Friendship Medical
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
16955739030310
Basic UDI
695573903002LB
Version Date
July 16, 2024
Manufacturer Last Update
May 11, 2021
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.9 Gao Xin 1st Road 710075 Xi'an
Email
george.zhai@friendshipmedical.com.cn
Authorized Representative
SRN
DK-AR-000001593
Country
Denmark
Address
3C Industrivej Roskilde
Email
erik.jensen@friendshipeurope.com
Telephone
+45 20164411
Regulatory Information
Competent Authority
Danish Medicines Agency, Pharmacovigilance & Medical Devices
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Italy
Market Available
Austria:2006-01-01~2099-12-31, Belgium:2006-01-01~2099-12-31, Bulgaria:2020-01-01~2099-12-31, Croatia:2020-01-01~2099-12-31, Cyprus:2006-01-01~2099-12-31, Czechia:2006-01-01~2099-12-31, Denmark:2006-01-01~2099-12-31, Estonia:2020-01-01~2099-12-31, Finland:2020-01-01~2099-12-31, France:2006-01-01~2099-12-31, Germany:2006-01-01~2099-12-31, Greece:2006-01-01~2099-12-31, Hungary:2020-01-01~2099-12-31, Iceland:2020-01-01~2099-12-31, Ireland:2006-01-01~2099-12-31, Italy:2006-01-01~2099-12-31, Latvia:2020-01-01~2099-12-31, Liechtenstein:2020-01-01~2099-12-31, Lithuania:2020-01-01~2099-12-31, Luxembourg:2020-01-01~2099-12-31, Malta:2020-01-01~2099-12-31, Netherlands:2020-01-01~2099-12-31, Norway:2006-01-01~2099-12-31, Poland:2020-01-01~2099-12-31, Portugal:2006-01-01~2099-12-31, Romania:2020-01-01~2099-12-31, Slovakia:2020-01-01~2099-12-31, Slovenia:2020-01-01~2099-12-31, Spain:2006-01-01~2099-12-31, Sweden:2006-01-01~2099-12-31, Türkiye:2020-01-01~2099-12-31, United Kingdom (Northern Ireland only):2020-01-01~2099-12-31
Device Characteristics
Human Tissues
No
Animal Tissues
No