Identity
- Trade Name
- LIFENET CONSULT INTERNATIONAL FDA UDI
- Generic Name
- Emergency/ambulatory healthcare software FDA UDI
- Device Name
- LIFENET CONSULT INTERNATIONAL RELEASE 5.3.3 FDA UDI
- Model / Reference
- 21340 FDA UDI
- Description
- LIFENET CONSULT INTERNATIONAL RELEASE 5.3.3 FDA UDI
Identifiers
- Catalog Number
- 21340-000838 FDA UDI
- Primary DI / UDI-DI
- 00883873863732 FDA UDI
- FDA Product Code
- MSX FDA UDI
- GMDN Term
- Emergency/ambulatory healthcare 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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Lifenet Consult International by PHYSIO-CONTROL, 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- PHYSIO-CONTROL, Inc.
Sources (1)
- FDA UDI 05c92164-348e-4d1a-a271-71347d903613 36 fields · synced Jun 9, 2026