FDA UDI
In Commercial Distribution
🇺🇸 United States
WALLSTENT™ RP Endoprosthesis
DI: 08714729345589
·
Model: M001712000
·
BOSTON SCIENTIFIC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- WALLSTENT™ RP Endoprosthesis
- Primary DI
- 08714729345589
- Version / Model
- M001712000
- Catalog Number
- M001712000
- Company Name
- BOSTON SCIENTIFIC CORPORATION
- Labeler DUNS
- 021717889
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2014-09-24
- Public Version
- 4
- Public Version Date
- 2021-02-05
- Public Version Status
- Update
- Public Device Record Key
- 1407433d-ef03-4e67-a48b-5f170fb4b62f
Device Description
Self-Expanding Stent
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
- No
- Has Lot/Batch Number
- Yes
- 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 |
|---|---|---|---|---|
| NIO | STENT, ILIAC | Unknown | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 44279 | Iliac artery stent, bare-metal | A non-bioabsorbable tubular device intended to be implanted in the common and/or external iliac artery(ies) to maintain arterial patency and luminal diameter in patients with symptomatic atherosclerotic disease. It is made of metal [e.g., stainless steel, nickel-titanium alloy (Nitinol)] and may be inserted with a balloon catheter which causes the device to expand when inflated, or it may self-expand after insertion with a delivery device. It may be a continuous tube or a mesh structure in tubular form and is available in a variety of lengths and diameters. Disposable devices associated with implantation may be included. | No | Obsolete |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 08714729345589 | GS1 |
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| P940019 | 000 |
| P940019 | 002 |
| P940019 | 003 |
| P940019 | 004 |
| P940019 | 005 |
| P940019 | 008 |
| P940019 | 009 |
| P940019 | 010 |
| P940019 | 011 |
| P940019 | 016 |
| P940019 | 019 |
| P940019 | 021 |
| P940019 | 025 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Device Size Text, specify | 6 mm Stent Diameter | ||
| Device Size Text, specify | 75 cm Effective Length | ||
| Device Size Text, specify | 24 mm Stent Length |