Identity
- Trade Name
- Pressure Monitor Tubing FDA UDI
- Generic Name
- Radiographic procedure tubing FDA UDI
- Model / Reference
- 00884450569726 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884450569726 FDA UDI
- FDA Product Code
- FPK FDA UDI
- GMDN Term
- Radiographic procedure tubing FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5440 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Radiographic procedure tubing
A comprehensive pressure monitor tubing is a flexible, cylindrical device designed to connect contrast imaging syringes to patient cannulas for medical procedures. It accommodates low and high pressures and is typically used in diagnostic radiographic procedures such as angiography or CT scans.
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Also classified as Radiographic procedure tubing.
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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 |
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Manufacturer
- Manufacturer
- Merit Medical Systems, Inc.
Sources (1)
- FDA UDI 0173fd3e-e8db-48ed-aaf5-9e02222f7044 33 fields · synced Oct 6, 2026