Norav NR Series

Kit includes: Norav Wireless 3In1 Acquisition Device NR2 (UDI: 7290110254872) for Resting-ECG combined with Respiration and Body-Movement - IEC type labelling. Input cable with 10 Patient…

Registry build 21.09.26

Kit includes: Norav Wireless 3In1 Acquisition Device NR2 (UDI: 7290110254872) for Resting-ECG combined with Respiration and Body-Movement – IEC type labelling. Input cable with 10 Patient leads IEC type and Banana connectors. Input cable with 5 Patient leads IEC type and Snap connectors.

4manufacturers in China registered for this device type
56catalogue numbers in this listing
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Shanghai (1), Beijing (1). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code MWJ
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Edan Instruments, Inc. Shenzhen Guangdong Contract manufacturer 56
Philips (China) Investment Co., Ltd. Philips Healthcare – Shanghai CDC Shanghai Shanghai Specification developer 6
DM Systems (Beijing) Co., Ltd. Beijing Beijing Manufacturer 1

Record

Regulatory record for Norav NR Series
Listed by Norav Medical Inc., United States
FDA product code MWJ
Device type Electrocardiograph, Ambulatory (Without Analysis)
Device class Class 2
Regulation 21 CFR 870.2800
Establishment Contract manufacturer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2019-09-30
Record revised 2019-11-08 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Label carries manufacturing date, serial number

Catalogue Numbers

Catalogue numbers for Norav NR Series
Catalogue number Size Status
NR1207 In distribution
NR1207 In distribution
NR1207-3 Kit In distribution
NR1207-3 In distribution
NR1207 In distribution
NR302 In distribution
NR1207-3 Kit In distribution
NR1207-E Kit In distribution
NR302 Kit In distribution
NR1207-3 In distribution
NR1207-E Kit In distribution
NR314T In distribution
NR1207-E Kit In distribution
NR314T In distribution
NR1207-E In distribution
NR1207-3 Kit In distribution
NR314 In distribution
NR1207-E Kit In distribution
NR314 In distribution
NR1207-E In distribution
NR1207-3 In distribution
NR1207 In distribution
NR302 In distribution
NR314 Kit In distribution
NR1207-3 In distribution
NR302 Kit In distribution
NR302 Kit In distribution
NR314 Kit In distribution
NR314T In distribution
NR302 Kit In distribution
NR314 Kit In distribution
NR1207-E Kit In distribution
NR314 Kit In distribution
NR314 Kit In distribution
NR1207 Kit In distribution
NR1207 Kit In distribution
NR314T Kit In distribution
NR1207-E Kit In distribution
NR1207-3 Kit In distribution
NR302 In distribution
NR314 In distribution
NR1207-3 Kit In distribution
NR302 In distribution
NR1207 Kit In distribution
NR314 Kit In distribution
NR314T In distribution
NR1207-E Kit In distribution
NR314 In distribution
NR1207-E In distribution
NR302 Kit In distribution
NR314 Kit In distribution
NR1207-3 In distribution
NR1207-E In distribution
NR302 Kit In distribution
NR302 Kit In distribution
NR1207-E In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Spacelabs Healthcare Spacelabs Healthcare (Washington), Inc 60
Welch Allyn, Inc. Welch Allyn, Inc. 58
Eclipse Pro Spacelabs Healthcare (Washington), Inc 25
Seer 1000 Getemed Medizin- UND Informationstechnik AG 15
Seer 1000 ECG Cable Getemed Medizin- UND Informationstechnik AG 12
ECG Cable for Seer 1000 Getemed Medizin- UND Informationstechnik AG 12
Seer Suzuken Co., Ltd. 12
H12+ Mortara Instrument, Inc. 10
Lifecard Spacelabs Healthcare (Washington), Inc 10
H3+ Patient Cable Mortara Instrument, Inc. 10
Spiderview Microport CRM SRL 9
ECG Cable for CM 3000-12 BT / Seer 12 Getemed Medizin- UND Informationstechnik AG 7

Showing 12 of 107. All products under Electrocardiograph, Ambulatory (Without Analysis)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K161062 2016-06-13

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer