Identity
- Trade Name
- LifeStent® Solo Vascular Stent FDA UDI
- Generic Name
- Peripheral artery stent, bare-metal FDA UDI
- Device Name
- LIFESTENT® SOLO™ Vascular Stent System 7 mm x 100 mm (135 cm delivery catheter) FDA UDI
- Model / Reference
- EX071003CL FDA UDI
- Description
- LIFESTENT® SOLO™ Vascular Stent System 7 mm x 100 mm (135 cm delivery catheter) FDA UDI
Identifiers
- Catalog Number
- EX071003CL FDA UDI
- Primary DI / UDI-DI
- 04049519004365 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
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
MR Conditional FDA UDI
LifeStent Solo Vascular Stent is a non-bioabsorbable, tubular device designed to provide permanent patency and improve luminal diameter in patients with atherosclerotic disease or following total occlusion.
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
- Bard Peripheral Vascular
Sources (1)
- FDA UDI c0f796be-de5a-492c-b389-ebb294744977 38 fields · synced Jul 19, 2026