Pure Global AI
EUDAMED registration 06972040112194Yes

Arm blood pressure monitor

Shenzhen AOJ Medical Technology Co., Ltd.Class IIaEU EUDAMEDTrade name: Arm Blood Pressure Monitor
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
Z1203020501
Trade name
Arm Blood Pressure Monitor
Implantable
No
Reusable
Yes
Measuring function
Yes
Registration information
Primary DI
06972040112194
Basic UDI
697204011AOJ30X17F
Version date
February 06, 2025
Manufacturer last update
August 01, 2022
Active status
Yes
Manufacturer
Country
China
Country type
NON_EU
Address
Shenzhen
Email
regulation@aojmedical.com
Authorized representative
SRN
DE-AR-000005132
Country
Germany
Address
12 Am Schulzentrum Kaarst
Email
eu-rep@share-info.com
Telephone
+49 01795666508
Regulatory information
Competent authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Market available
France:2024-03-25~2025-03-25, Germany:2024-03-25~2025-03-25, Italy:2024-03-25~2025-03-25, United Kingdom (Northern Ireland only):2024-03-25~2025-03-25
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

NON–INVASIVE OSCILLOMETRIC BLOOD PRESSURE GAUGES

About this record

Access comprehensive regulatory information for Arm blood pressure monitor 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 06972040112194 and manufactured by Shenzhen AOJ Medical Technology Co., Ltd. in China.

This page provides complete registration details including trade name (Arm Blood Pressure Monitor), manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Düsseldorf Dezernat 24), 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.