FDA UDI
Not in Commercial Distribution
🇺🇸 United States
Sentry IVC Filter
DI: 05391529380069
·
Model: 146155-01
·
NOVATE MEDICAL LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1
Basic Information
- Brand Name
- Sentry IVC Filter
- Primary DI
- 05391529380069
- Version / Model
- 146155-01
- Catalog Number
- NM60-16-28
- Company Name
- NOVATE MEDICAL LIMITED
- Labeler DUNS
- 896415242
- Distribution Status
- Not in Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2018-09-27
- Public Version
- 4
- Public Version Date
- 2022-10-11
- Public Version Status
- Update
- Public Device Record Key
- 41f8a47f-e5d1-4f41-a95a-f27d075a4e8b
- Distribution End Date
- 2022-10-10
Device Description
The Sentry IVC Filter is indicated for the prevention of recurrent Pulmonary Embolism via percutaneous placement in the inferior vena cava in patients at transient risk of PE, in the following situations: • Pulmonary thromboembolism when anticoagulants are contraindicated. • Failure of anticoagulant therapy in thromboembolic diseases. • Emergency treatment following massive PE where anticipated benefits of conventional therapy are reduced.
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 |
|---|---|---|---|---|
| DTK | Filter, Intravascular, Cardiovascular | Cardiovascular | 870.3375 | 2 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 44864 | Vena cava filter, temporary/permanent | A vascular device intended to be percutaneously implanted in the inferior vena cava (IVC) to prevent pulmonary embolism (PE); it can be retrieved before a threshold period or remain as a permanent implant after the period. It achieves its unconstrained diameter upon deployment in the IVC and imparts an outward radial force on the luminal surface of the vena cava to ensure proper positioning and stability. It is designed for blood clot capture while maintaining caval patency. It is made of metal alloys [e.g., stainless steel, titanium (Ti), nickel-titanium alloy (Nitinol)] and is available in various self-expanding designs (e.g., conical, basket). This is a single-use device. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Package | 05391529380076 | GS1 | 5 | Not in Commercial Distribution | 2022-10-10 | |
| Primary | 05391529380069 | GS1 |