Identity
- Trade Name
- Waveline EZ+ FDA UDI
- Generic Name
- Pulse oximeter, line-powered FDA UDI
- Model / Reference
- 60144IBP FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815871020930 FDA UDI
- FDA Product Code
- DSI FDA UDIDQA FDA UDI
- GMDN Term
- Pulse oximeter, line-powered FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1025 FDA UDI870.2700 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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: General-purpose multi-parameter bedside monitorPulse oximeter, line-powered
Waveline EZ+ by Avante — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Pulse oximeter, line-powered.
- BCI — ICU MEDICAL, INC. · Class II
- Reusable Sensor - Y — MEDIAID INC · Class II
- Reusable Sensor - Ear — MEDIAID INC · Class II
- Unimed — Unimed Medical Supplies, Inc. · Class II
- BCI — ICU MEDICAL, INC. · Class II
- BCI — ICU MEDICAL, INC. · Class II
- Caring Mill — Caring Mill · Class II
- Reusable Sensor - Compushield (SCS) — MEDIAID 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
- Avante
Sources (1)
- FDA UDI 43c48838-28e2-4a15-85bb-140b2226588d 33 fields · synced May 30, 2026