Identity
- Trade Name
- Stat Profile FDA UDI
- Generic Name
- Co-oximetry analyser IVD, point-of-care FDA UDI
- Device Name
- Flow Path Flush Tool FDA UDI
- Model / Reference
- Prime FDA UDI
- Description
- Flow Path Flush Tool FDA UDI
Identifiers
- Catalog Number
- 53443 FDA UDI
- Primary DI / UDI-DI
- 00385480534437 FDA UDI
- FDA Product Code
- CHL FDA UDI
- GMDN Term
- Co-oximetry analyser IVD, point-of-care FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1120 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Blood gas/haemoximetry analyser IVD, point-of-careBlood gas analyser IVD, point-of-careCo-oximetry analyser IVD, point-of-care
Stat Profile by Nova Biomedical Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Co-oximetry analyser IVD, point-of-care.
- Avoximeter Whole Blood CO-Oximeter — ACCRIVA DIAGNOSTICS HOLDINGS, INC. · Class I
- Avoximeter Whole Blood CO-Oximeter — ACCRIVA DIAGNOSTICS HOLDINGS, INC. · Class I
- Specials — SeaSpine Orthopedics Corporation · Class I
- Avoximeter Whole Blood CO-Oximeter — ACCRIVA DIAGNOSTICS HOLDINGS, INC. · Class I
- Avoximeter Whole Blood Oximeter — ACCRIVA DIAGNOSTICS HOLDINGS, INC. · Class II
- Specials — SeaSpine Orthopedics Corporation · Class I
- Specials — SeaSpine Orthopedics Corporation · Class I
- Avoximeter Whole Blood Oximeter — ACCRIVA DIAGNOSTICS HOLDINGS, 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
- Nova Biomedical Corporation
Sources (1)
- FDA UDI baea1b36-0cff-448c-bede-a60f8cd45179 35 fields · synced Jun 8, 2026