Identity
- Trade Name
- TIGRIS Vascular Stent FDA UDI
- Generic Name
- Peripheral artery stent, bare-metal FDA UDI
- Model / Reference
- PHA050401A FDA UDI
Identifiers
- Catalog Number
- PHA050401A FDA UDI
- Primary DI / UDI-DI
- 00733132636129 FDA UDI
- PMA Number
- P160004 FDA UDI
- FDA Product Code
- NIP FDA UDI
- GMDN Term
- Peripheral artery stent, bare-metal FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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
Yes
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Catheter Gauge — 6 French FDA UDILumen/Inner Diameter — 5 Millimeter FDA UDILength — 40 Millimeter FDA UDI
TIGRIS Vascular Stent by W. L. Gore & Associates, Inc — Class III — 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 III | Pending data |
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Manufacturer
- Manufacturer
- W. L. Gore & Associates, Inc
Sources (1)
- FDA UDI 62771fd2-bf45-458e-8987-335558166ae2 37 fields · synced Jun 1, 2026