FDA device listing
Disposable Angled Mouthpiece,Mouthpiece, Angled,Mouthpiece Straight,Reusable Mouthpiece
FDA device listing 1835073509 · Philips Medical Systems International BV
Key facts
| Proprietary names | Disposable Angled Mouthpiece,Mouthpiece, Angled,Mouthpiece Straight,Reusable Mouthpiece |
|---|---|
| Owner/operator | Philips Medical Systems International BV |
| Owner/operator number | 2518422 |
| Product codes | BYP |
| Device names | BYP - Mouthpiece, Breathing |
| Device class | Class I |
| Classification regulations (21 CFR) | 868.5620 |
| Review panels | Anesthesiology |
| Registered establishments | RESPIRONICS INC., Respironics Medical Products (Shenzhen) Co., Ltd. |
| Establishment registrations | 2518422, 3038562397 |
| FEI numbers | 2518422, 3038562397 |
| Establishment operations | Complaint File Establishment, Specification Developer, Contract Manufacturer |
| Registration valid through | 2026 |
At a glance
- 1–9 Registered establishments listing this device
- None listed 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