Identity
- Trade Name
- Surveyor S4 FDA UDI
- Generic Name
- Centralized patient monitor FDA UDI
- Device Name
- Electrocardiographic telemetry monitoring system transmitter FDA UDI
- Model / Reference
- S4-P-B FDA UDI
- Description
- Electrocardiographic telemetry monitoring system transmitter FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00812345024661 FDA UDI
- FDA Product Code
- MHX FDA UDIDRG FDA UDI
- GMDN Term
- Centralized patient monitor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1025 FDA UDI870.2910 FDA UDI
- Commercial Distribution
- Not 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
No
FDA UDI
Surveyor S4 by Mortara Instrument, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Mortara Instrument, Inc.
Sources (1)
- FDA UDI 029a2109-31b1-47ec-925c-fe7c13a6894b 36 fields · synced Jun 1, 2026