Compumedics Grael

Grael v2 System with PSG software

Registry build 21.09.26
1manufacturer
6catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Registered in Jiangsu. One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code OLV
Manufacturer City Province Registered as Device types
Jiangyin Sinbon Electronics Co Ltd Jiangyin Jiangsu Contract manufacturer 13

Record

Regulatory record for Compumedics Grael
Listed by Compumedics Limited, Australia
FDA product code OLV
Device type Standard Polysomnograph With Electroencephalograph
Device class Class 2
Regulation 21 CFR 882.1400
Establishment Complaint-file establishment, Manufacturer, Exporter
510(k) K093223
Record published 2016-11-29
Record revised 2022-11-28 (version 5)

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
Storage Storage environment humidity 20 to 90 % RH; Storage environment temperature -10 to 50 °C
Packaging Box of 5

Catalogue Numbers

Catalogue numbers for Compumedics Grael
Catalogue number Size Status
Grael PSG In distribution
Grael LT In distribution
Grael In distribution
Grael PSG In distribution
Grael PSG In distribution
Grael In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Alice 6 Respironics Inc. 58
Somnostar Carefusion 28
Standard Polysomnograph With Electroencephalograph Nihon Kohden America, Inc. 18
Standard Polysomnograph With Electroencephalograph Nihon Kohden Corp. 17
Sleep Profiler PSG2 Advanced Brain Monitoring, Inc. 10
Sleep Profiler Advanced Brain Monitoring, Inc. 8
Trackit Sleepwalker Lifelines Ltd. 8
micromed Micromed, Inc. 7
Neurovirtual Neurovirtual USA, Inc. 4
Pro-Flow Respironics Inc. 3
Serenity TH01 Thermocouple Sensor w/ Hanger, 1.5mm DIN, 2.0m Neurotronics, LLC 3
Xltek Embla Systems 3

Showing 12 of 89. All products under Standard Polysomnograph With Electroencephalograph

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242447 2025-02-20
K003175 2000-12-27

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