FDA device listing
PHILIPS INTELLIVUE TCG10
FDA device listing 1640907827 · DHL Supply Chain (Netherlands) B.V.
Key facts
| Proprietary names | PHILIPS INTELLIVUE TCG10 |
|---|---|
| Owner/operator | DHL Supply Chain (Netherlands) B.V. |
| Owner/operator number | 10085309 |
| Premarket submissions | K110474 |
| Product codes | KLK, LKD, LPP |
| Device names | KLK - Monitor, Oxygen, Cutaneous, For Infant Not Under Gas Anesthesia, LKD - Monitor, Carbon-Dioxide, Cutaneous, LPP - Monitor, Oxygen, Cutaneous, For Uses Other Than For Infant Not Under Gas Anesthesia |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.2480, 868.2500 |
| Review panels | Anesthesiology |
| Registered establishments | DHL SUPPLY CHAIN (NETHERLANDS) B.V. |
| Establishment registrations | 3009077524 |
| FEI numbers | 3009077524 |
| Establishment operations | Foreign Exporter |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- 1–9 UDI devices (GUDID) under the same submission
- 1–9 Device listings citing the same submission
- Yes Premarket submission listed
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device listings
Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database