Identity
- Trade Name
- AngioDynamics FDA UDI
- Generic Name
- Peripheral vascular guidewire, manual FDA UDI
- Device Name
- STRAIGHT TIP, FIXED CORE, PTFE COATED FDA UDI
- Model / Reference
- 05500202 FDA UDI
- Description
- STRAIGHT TIP, FIXED CORE, PTFE COATED FDA UDI
Identifiers
- Primary DI / UDI-DI
- H787055002021 FDA UDI
- FDA Product Code
- DQX FDA UDI
- GMDN Term
- Peripheral vascular guidewire, manual FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 870.1330 FDA UDI
- Commercial Distribution
- Not 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
- Length — 150 Centimeter FDA UDIOuter Diameter — 0.035 Inch FDA UDI
AngioDynamics by Angiodynamics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 e3df81ba-abc9-4882-926f-bd6c19e1116b 37 fields · synced Jun 8, 2026