FDA UDI
In Commercial Distribution
🇺🇸 United States
Vela Proximal Endograft System
DI: 00818009013606
·
Model: A34-34/C80-O20 V
·
ENDOLOGIX, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Vela Proximal Endograft System
- Primary DI
- 00818009013606
- Version / Model
- A34-34/C80-O20 V
- Company Name
- ENDOLOGIX, INC.
- Labeler DUNS
- 858560477
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2014-09-24
- Public Version
- 8
- Public Version Date
- 2023-01-10
- Public Version Status
- Update
- Public Device Record Key
- 06d1d5b6-68ff-40ca-86b0-ae415436e3c5
Device Characteristics
- Single Use
- Yes
- Prescription Use (Rx)
- Yes
- Over the Counter (OTC)
- No
- Kit
- No
- Combination Product
- No
- HCT/P
- No
- Contains NRL
- No
- Not Made with NRL
- No
- MRI Safety
- MR Conditional
- Direct Marking Exempt
- No
- PM Exempt
- No
- Has Serial Number
- Yes
- Has Lot/Batch Number
- No
- Has Manufacturing Date
- No
- Has Expiration Date
- Yes
- Has Donation ID
- No
Sterilization
- Is Sterile
- Yes
- Sterilization Prior Use
- No
Product Codes
| Code | Name | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| MIH | System, Endovascular Graft, Aortic Aneurysm Treatment | Unknown | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46777 | Abdominal aorta endovascular stent-graft | A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA); it does not contain anticoagulants or pharmaceuticals that prevent narrowing of the vessels. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is typically made of a metallic outer mesh structure with an inner polymer tube (endovascular graft) and is typically available in two designs: 1) a single tube for insertion into one iliac artery; or 2) a two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00818009013606 | GS1 |
Customer Contacts
- Phone
- (949) 595-7200
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| P040002 | 041 |
| P040002 | 042 |
| P040002 | 043 |
| P040002 | 044 |
| P040002 | 045 |
| P040002 | 046 |
| P040002 | 047 |
| P040002 | 048 |
| P040002 | 050 |
| P040002 | 051 |
| P040002 | 052 |
| P040002 | 053 |
| P040002 | 054 |
| P040002 | 056 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 34 mm, Proximal Diameter | ||
| Device Size Text, specify | 34 mm, Distal Diameter | ||
| Device Size Text, specify | 80 mm, Covered Extension Length | ||
| Device Size Text, specify | 20 mm, Uncovered Extension Length |