Identity
- Trade Name
- Merit Medical® FDA UDI
- Generic Name
- Radiographic procedure tubing FDA UDI
- Model / Reference
- 00884450052846 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00884450052846 FDA UDI
- FDA Product Code
- OJA 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
Yes
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
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 flexible, cylindrical device that connects a contrast imaging syringe to a patient cannula for the conduction of contrast media and flushing fluids during diagnostic radiographic procedures. It is made of synthetic polymers, accommodates low and high pressures, and comes in various lengths with quick connecting fittings.
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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 193d7b0a-c75e-43fe-948f-122c34434494 32 fields · synced Jul 19, 2026