Identity
- Trade Name
- Uni-Fuse+ FDA UDI
- Generic Name
- Peripheral vascular intervention infusion catheter FDA UDI
- Device Name
- Uni-Fuse+ Infusion System 5F, 135cm, 10cm FDA UDI
- Model / Reference
- H787124018490 FDA UDI
- Description
- Uni-Fuse+ Infusion System 5F, 135cm, 10cm FDA UDI
Identifiers
- Catalog Number
- 12401849 FDA UDI
- Primary DI / UDI-DI
- 15051684023832 FDA UDI
- 510(k) Number
- K202347 FDA UDI
- FDA Product Code
- KRA FDA UDI
- GMDN Term
- Peripheral vascular intervention infusion catheter FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1210 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
Dimensions & Sizes
- Size
- Outer Diameter — 1.71 Millimeter FDA UDILength — 135 Centimeter FDA UDICatheter Gauge — 5 French FDA UDI
Category: Peripheral vascular intervention infusion catheter
Uni-Fuse+ by Angiodynamics, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K202347 also covers:
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC
- Uni-Fuse+ — ANGIODYNAMICS, INC.
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
- Angiodynamics, Inc
Sources (1)
- FDA UDI 1b3fe124-968f-4e30-b72d-f3ea6f1027e0 38 fields · synced Jun 20, 2026