LifeStream
- Primary DI
- 05391522080997
- Brand
- LifeStream
- Company
- CLEARSTREAM TECHNOLOGIES LIMITED
- Model
- LSMU1350537
- Catalog number
- LSMU1350537
- Device description
- LifeStream™ Balloon Expandable Vascular Covered Stent, 5 mm x 37 mm, 135 cm catheter length
- Published
- 2017-04-26
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Related Records
Contact Domains
Product Codes
| Code | Name |
|---|---|
| PRL | Iliac covered stent, arterial |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|---|---|---|
| PRL | Iliac Covered Stent, Arterial | Unknown | 3 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 05391522080997 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|---|---|
| 05391522080997 | 05391522080997 | 5391522080997 |
GMDN Terms
| Term | Definition |
|---|---|
| Iliofemoral artery endovascular stent-graft | A sterile non-bioabsorbable tubular device intended to be implanted in the iliac and, alternatively, superficial femoral arteries to reline tortuous arteries in patients with symptomatic peripheral vascular disease (PVD). It is percutaneously inserted via the femoral artery to the site of implantation, with a disposable delivery device, where it self-expands. It is typically made of nickel-titanium alloy (Nitinol) that forms an outer mesh structure with an inner polymer tube (endovascular graft). It is available in a variety of lengths and diameters. Disposable devices associated with implantation may be included. |
Device Sizes
| Type | Value | Unit |
|---|---|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 |
Sterilization Methods
| Method |
|---|
Contacts
| Phone | |
|---|---|
| +1(800)321-4254 | medical.services@crbard.com |
Regulatory Flags
- DUNS number
- 989214291
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- true
- Sterilization required before use
- false
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