FDA device listing
Ispira Resuscitation System Circuit; NeoPIP Neonatal Resuscitation Kit; NeoPIP Resuscitation Circuit with PEEP
FDA device listing 1452471947 · FLEXICARE MEDICAL LTD.
Key facts
| Proprietary names | Ispira Resuscitation System Circuit; NeoPIP Neonatal Resuscitation Kit; NeoPIP Resuscitation Circuit with PEEP |
|---|---|
| Owner/operator | FLEXICARE MEDICAL LTD. |
| Owner/operator number | 8021995 |
| Premarket submissions | K103833 |
| Product codes | BYE |
| Device names | BYE - Attachment, Breathing, Positive End Expiratory Pressure |
| Device class | Class II |
| Classification regulations (21 CFR) | 868.5965 |
| Review panels | Anesthesiology |
| Registered establishments | Flexicare Lanka (Pvt) Ltd, FLEXICARE MEDICAL (DONGGUAN) LTD., FLEXICARE MEDICAL LTD. |
| Establishment registrations | 8021995, 3006061749, 3017202422 |
| FEI numbers | 3006061749, 3006363476, 3017202422 |
| Establishment operations | Contract Manufacturer, Specification Developer |
| 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