Bendini
- Primary DI
- 00887517605078
- Brand
- Bendini
- Company
- Nuvasive, Inc.
- Model
- 8210314
- Device description
- Bendini ASF Pointer
- Published
- 2018-09-21
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| ETN | Stimulator, Nerve | Ear, Nose, Throat | 2 |
| GWF | Stimulator, Electrical, Evoked Response | Neurology | 2 |
| HAW | Neurological Stereotaxic Instrument | Neurology | 2 |
| IKN | Electromyograph, Diagnostic | Physical Medicine | 2 |
| OLO | Orthopedic Stereotaxic Instrument | Neurology | 2 |
| PDQ | Neurosurgical Nerve Locator | Ear, Nose, Throat | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K143641 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887517605078 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887517605078 | 00887517605078 | 887517605078 | 0887517605078 |
GMDN Terms#
| Term | Definition |
|---|---|
| Spinal rod bending system | An assembly of mains electricity (AC-powered) computerized devices intended to be used to determine the relative locations of internal spinal fixation system implants (e.g., screws, hooks) for the production of bend instructions to shape a spinal rod during spinal fusion surgery. It primarily consists of an electronic spatial measurement system used with manual tools to determine implant location and to take measurements; computer/software to convert implant locations to a series of bend instructions; and an orthopaedic rod bender to execute bend instructions. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| +1(858)909-1800 | RA_UDI@nuvasive.com |
| +1800-475-9131 | nuvainfo@globusmedical.com |
Regulatory Flags#
- DUNS number
- 053950783
- Device count
- 1
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00887517614360 | Propel | 5020001 | 2015-09-24 | |
| 00887517614377 | Propel | 5020005 | 2015-09-24 | |
| 00887517614384 | Propel | 5020010 | 2015-09-24 | |
| 00887517939951 | AttraX | 5015110 | 2018-06-05 | |
| 00887517939968 | AttraX | 5015120 | 2018-06-05 | |
| 00887517939975 | AttraX | 5015130 | 2018-06-05 | |
| 00887517939982 | AttraX | 5015103 | 2018-06-05 | |
| 00887517939999 | AttraX | 5015104 | 2018-06-05 | |
| 00887517940001 | AttraX | 5015106 | 2018-06-05 | |
| 00887517940018 | AttraX | 5015101 | 2018-06-05 | |
| 00887517940025 | AttraX | 5015102 | 2018-06-05 | |
| 00887517970435 | Propel | 5020205 | 2018-12-20 | |
| 00887517970442 | Propel | 5020205994 | 2018-12-20 | |
| 00887517970459 | Propel | 5020210 | 2018-12-20 | |
| 00887517970466 | Propel | 5020210994 | 2018-12-20 | |
| 00887517970473 | Propel | 5020301 | 2018-12-20 | |
| 00887517970480 | Propel | 5020301994 | 2018-12-20 | |
| 00887517970497 | Propel | 5020305 | 2018-12-20 | |
| 00887517971500 | Propel | 5020305994 | 2018-12-20 | |
| 00887517971517 | Propel | 5020310 | 2018-12-20 |
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| 07340201503867 | Leksell Neurosurgical Instruments | Elekta Solutions AB | HAW | 2026-10-20 |
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