Identity
- Trade Name
- Vital Signs™ FDA UDI
- Generic Name
- Injectate temperature probe FDA UDI
- Device Name
- Cardiac output in-line injectate probe for GE monitors, ICU Medical Thermoset, 2.4 m/8 ft FDA UDI
- Model / Reference
- 9446-913 FDA UDI
- Description
- Cardiac output in-line injectate probe for GE monitors, ICU Medical Thermoset, 2.4 m/8 ft FDA UDI
Identifiers
- Catalog Number
- 9446-913 FDA UDI
- Primary DI / UDI-DI
- 10190752125636 FDA UDI
- FDA Product Code
- DQE FDA UDI
- GMDN Term
- Injectate temperature probe FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1230 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Injectate temperature probe
Vital Signs™ by Airlife, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Injectate temperature probe.
- IN-LINE INJECTATE SENSOR CABLE-SP4046-1 — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- IN-LINE INJECTATE SENSOR CABLE-SP4044-1S 36IN — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- Roydent — ROYDENT DENTAL PRODUCTS INC · Class II
- CATHETER CONN CABLE-SP4035-1 — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- IN-LINE INJECTATE SENSOR CABLE-SP4046 — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- IN-LINE INJECTATE SENSOR CABLE-SP4045 — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- IN-LINE INJECTATE SENSOR CABLE-SP4042 — ARGON CRITICAL CARE SYSTEMS SINGAPORE PTE. LTD. · Class II
- Roydent — ROYDENT DENTAL PRODUCTS INC · Class II
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
- Airlife, Inc.
Sources (1)
- FDA UDI ae336999-a24a-4280-9037-b15e7ea7714a 36 fields · synced May 30, 2026