KC 9-P Auto-PEEP Measurement Device
- Primary DI
- M996KC9P0
- Brand
- KC 9-P Auto-PEEP Measurement Device
- Company
- INSTRUMENTATION INDUSTRIES, INCORPORATED
- Model
- KC 9-P
- Device description
- The KC 9-P with removable cap is designed for use on ventilators not equipped with expiratory hold. It allows single breath measurement of auto-PEEP in its use as a Braschi valve.Objectives of PEEP therapy: 1) increase functional residual capacity by maintaining a positive pressure throughout the ventilatory cycle - improves gas distribution,2) aid in the prevention of atelectasis via aveolar stinting, 3) decrease in the inspired oxygen fraction (FiO2) is an advantage, 4) help in the stabilization of flail chest condition, and 5) monitor tidal volume by connecting a spirometer to the outlet port.
- Published
- 2015-10-22
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| CBP | Valve, Non-Rebreathing |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| CBP | Valve, Non-Rebreathing | Anesthesiology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K983631 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| M996KC9P2 | Package | HIBCC | 10 | In Commercial Distribution |
| M996KC9P0 | Primary | HIBCC | 0 |
GMDN Terms#
| Term | Definition |
|---|---|
| Non-rebreathing valve, single-use | A non-sterile device containing a one-way valve intended to be used to direct the flow of breathing gases, typically in a breathing circuit or between an oxygen mask and its reservoir bag, to prevent patient rebreathing of exhaled gases. The device is available in various designs and includes unidirectional valves made of various materials (e.g., silicone, rubber, metal, or mica sheets/discs) that typically open and close with each inspiration/expiration. This is a single-use device. |
Sterilization Methods#
| Method |
|---|
| High-level Disinfectant |
Contacts#
| Phone | |
|---|---|
| 412-854-1133 | raqa@iiimedical.com |
Regulatory Flags#
- DUNS number
- 053146767
- Device count
- 1
- Lot or batch
- true
- No natural rubber latex
- true
- Sterilization required before use
- true
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