← Back to catalogue
Philips HeartStart Telemedicine Additional Viewer Client License
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Philips HeartStart Telemedicine Additional Viewer Client License FDA UDI
- Generic Name
- Cardiology information system application software FDA UDI
- Device Name
- Philips HeartStart Telemedicine Additional Viewer Client License FDA UDI
- Model / Reference
- 861453 FDA UDI
- Description
- Philips HeartStart Telemedicine Additional Viewer Client License FDA UDI
Identifiers
- Catalog Number
- 861453 FDA UDI
- Primary DI / UDI-DI
- 00884838041530 FDA UDI
- FDA Product Code
- MSX FDA UDI
- GMDN Term
- Cardiology information system application software FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.2300 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
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Philips HeartStart Telemedicine Additional Viewer Client License by Philips Electronics North America Corporation — Class II — FDA UDI — listed in FDA GUDID
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Philips Electronics North America Corporation
Sources (1)
- FDA UDI 07377b69-e86b-4dcf-b84b-abca7fd47633 35 fields · synced May 31, 2026