Identity
- Trade Name
- ADVANCED PATIENT MONITOR FDA UDI
- Generic Name
- Multiple vital physiological parameter monitoring system, clinical FDA UDI
- Model / Reference
- PM-Max15 FDA UDI
Identifiers
- Primary DI / UDI-DI
- B510PMMAX15 FDA UDI
- FDA Product Code
- MLD FDA UDICCK FDA UDIDSF FDA UDIDSI FDA UDIDQA FDA UDIDXN FDA UDIDRT FDA UDICCL FDA UDIFLL FDA UDICBS FDA UDICBR FDA UDIMHX FDA UDIDSA FDA UDIDSK FDA UDICBQ FDA UDI
- GMDN Term
- Multiple vital physiological parameter monitoring system, clinical FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1025 FDA UDI868.1400 FDA UDI870.2810 FDA UDI870.2700 FDA UDI870.1130 FDA UDI870.2300 FDA UDI868.1720 FDA UDI880.2910 FDA UDI868.1620 FDA UDI868.1700 FDA UDI870.2900 FDA UDI870.1110 FDA UDI868.1500 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
No
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
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Multiple vital physiological parameter monitoring system, clinical
Advanced Patient Monitor by Advanced Instrumentations, Inc. — 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
- Advanced Instrumentations, Inc.
Sources (1)
- FDA UDI 87b929ac-9f78-420d-bccb-3b63074f354f 32 fields · synced May 30, 2026