Catalogue number 862293, listed by Philips Medizin Systeme Böblingen GmbH, Germany, under Full-Montage Standard Electroencephalograph. 3 manufacturers in China are registered for this product code.
Who Else Makes It
Concentrated in Guangdong (1), Jiangsu (1), Shaanxi (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
Record
Regulatory record for Philips BIS Module | Listed by | Philips Medizin Systeme Böblingen GmbH, Germany |
| FDA product code | GWQ |
| Device type | Full-Montage Standard Electroencephalograph |
| Device class | Class 2 |
| Regulation | 21 CFR 882.1400 |
| Record published | 2017-01-03 |
| Record revised | 2020-12-07 (version 4) |
Specifications
Specifications | MRI safety | MR Unsafe |
| Label carries | serial number |
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.