Catalogue number 862283, listed by Philips Medizin Systeme Böblingen GmbH, Germany, under Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia. 1 manufacturer in China is registered for this product code.
Who Else Makes It
Registered in Guangdong. One is registered as a contract manufacturer, able to build to a specification.
Record
Regulatory record for Philips Transcutaneous pO2/pCO2 Parameter Module | Listed by | Philips Medizin Systeme Böblingen GmbH, Germany |
| FDA product code | KLK |
| Device type | Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia |
| Device class | Class 2 |
| Regulation | 21 CFR 868.2500 |
| Record published | 2016-11-02 |
| 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.