FDA UDI
In Commercial Distribution
🇺🇸 United States
Neuroform3
DI: 07613252193937
·
Model: M003SNF345200
·
Stryker Corporation
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- Neuroform3
- Primary DI
- 07613252193937
- Version / Model
- M003SNF345200
- Catalog Number
- M003SNF345200
- Company Name
- Stryker Corporation
- Labeler DUNS
- 042405446
- Distribution Status
- In Commercial Distribution
- Device Count in Pkg
- 1
- Record Status
- Published
- Publish Date
- 2015-05-29
- Public Version
- 7
- Public Version Date
- 2021-02-05
- Public Version Status
- Update
- Public Device Record Key
- 1061265a-772c-482f-9933-e54b3a706be8
Device Description
Microdelivery Stent System
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 |
|---|---|---|---|---|
| NJE | intracranial neurovascular stent | Unknown | f |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 46352 | Bare-metal intracranial vascular stent | A non-bioabsorbable tubular device typically intended to be implanted into the base or parent artery of an intracranial aneurysm (e.g., wide-neck aneurysm situated at the base of a bifurcation) to facilitate the delivery of embolics to fill the aneurysm, facilitate clotting within the aneurysm by slowing blood flow into it, and/or to provide support for a neurovascular embolization coil placed inside the aneurysm. It is made of uncoated metal [e.g., nickel-titanium alloy (Nitinol)] and self-expands after it is delivered to the site of implantation and released (e.g., from a dedicated delivery instrument). Disposable devices associated with implantation may be included. | Yes | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 07613252193937 | GS1 |
Customer Contacts
- Phone
- +1(855)916-3876
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| H020002 | 001 |
| H020002 | 002 |
| H020002 | 004 |
| H020002 | 005 |
| H020002 | 006 |
| H020002 | 007 |
| H020002 | 008 |
| H020002 | 011 |
| H020002 | 012 |
| H020002 | 013 |
| H020002 | 014 |
| H020002 | 015 |
| H020002 | 017 |
| H020002 | 020 |
| H020002 | 021 |
| H020002 | 022 |
| H020002 | 025 |
| H020002 | 027 |
| H020002 | 029 |
| H020002 | 030 |
| H020002 | 032 |
| H020002 | 033 |
| H020002 | 034 |
| H020002 | 036 |
| H020002 | 039 |
| H020002 | 040 |
| H020002 | 041 |
| H020002 | 042 |
| H020002 | 043 |
| H020002 | 045 |
| H020002 | 047 |
| H020002 | 049 |
| H020002 | 050 |
| H020002 | 053 |
| H020002 | 054 |
| H020002 | 055 |
Device Sizes
| Type | Value | Unit | Text |
|---|---|---|---|
| Length | 20.0 | Millimeter | |
| Outer Diameter | 4.5 | Millimeter |
Storage Conditions
- Type
- Special Storage Condition, Specify
- Special Conditions
- Store in cool, dry, dark place.