Identity
- Trade Name
- Nightingale Monitoring System FDA UDI
- Generic Name
- Multiple vital physiological parameter monitoring system, clinical FDA UDI
- Device Name
- The Nightingale PPM3 Monitor is intended for monitoring, recording, and alarming basic vital signs on adult and pediatric patients. FDA UDI
- Model / Reference
- Nightingale PPM3 FDA UDI
- Description
- The Nightingale PPM3 Monitor is intended for monitoring, recording, and alarming basic vital signs on adult and pediatric patients. FDA UDI
Identifiers
- Catalog Number
- 179-0003 FDA UDI
- Primary DI / UDI-DI
- 00851920007040 FDA UDI
- 510(k) Number
- K130740 FDA UDI
- FDA Product Code
- MWI FDA UDI
- GMDN Term
- Multiple vital physiological parameter monitoring system, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2300 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
Category: Multiple vital physiological parameter monitoring system, clinical
Nightingale Monitoring System by Zoe Medical Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Zoe Medical Incorporated
Sources (1)
- FDA UDI 1975d146-b2ec-4c80-8be1-2e984c3cb6c6 37 fields · synced Jun 8, 2026