Bendini
- Primary DI
- 00887517141132
- Brand
- Bendini
- Company
- Nuvasive, Inc.
- Model
- 1578787
- Device description
- Bendini IR Probe Passive Sphere, 5 Pack
- Published
- 2019-07-15
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- Single use
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| OLO | Orthopedic stereotaxic instrument |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| OLO | Orthopedic Stereotaxic Instrument | Neurology | 2 |
Premarket Submissions#
| Submission | Supplement |
|---|---|
| K111811 | 000 |
Premarket Details#
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00887517141132 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00887517141132 | 00887517141132 | 887517141132 | 0887517141132 |
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 |
|---|
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
- Manufacturing date on label
- true
- Expiration date on label
- 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 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
| 04056481147969 | Spine and Trauma Navigation | Brainlab SE | OLO | 2026-10-19 |
| 00889024713390 | ROSA® Shoulder | Orthosoft Inc | OLO | 2026-10-15 |
| 00885556919781 | Real Intelligence | Smith & Nephew, Inc. | OLO | 2026-10-13 |
| 10705034648194 | VELYS | Medos International Sàrl | OLO | 2026-10-09 |
| 10705034648200 | VELYS | Medos International Sàrl | OLO | 2026-10-09 |
| 00885556924327 | Real Intelligence | Smith & Nephew, Inc. | OLO | 2026-10-08 |
| 00889024673403 | NavitrackER® | Orthosoft Inc | OLO | 2026-06-26 |
| 04056481146702 | Curve Navigation | Brainlab SE | OLO | 2025-10-13 |
| 07613327631814 | RPS | Stryker Leibinger GmbH & Co. KG | OLO | 2025-10-03 |
| 04056481146054 | Patient Reference Rod-Clamp Spine & Trauma | Brainlab SE | OLO | 2025-09-19 |
| 04056481145439 | PATIENT REFERENCE STEEL-CLAMP SPINE & TRAUMA SIZE S | Brainlab SE | OLO | 2025-06-17 |
| 04056481145446 | PATIENT REFERENCE STEEL-CLAMP SPINE & TRAUMA SIZE L | Brainlab SE | OLO | 2025-06-17 |
| 07613252196259 | FLUOROMAP | Stryker Leibinger GmbH & Co. KG | OLO | 2025-01-28 |
| 07613252286622 | FLUOROMAP | Stryker Leibinger GmbH & Co. KG | OLO | 2025-01-28 |
| 04056481144906 | Spine &Trauma Navigation | Brainlab SE | OLO | 2024-11-14 |
| 04056481146238 | PATIENT REFERENCE ARRAY SPINE & TRAUMA | Brainlab SE | OLO | 2024-11-14 |
| 04056481146603 | ADAPTER SHORT FOR PATIENT REFERENCE CLAMP | Brainlab SE | OLO | 2024-11-14 |
| 04056481146610 | ADAPTER X-PRESS FOR PATIENT REFERENCE ARRAY | Brainlab SE | OLO | 2024-11-14 |
| 04056481144753 | Drill Guide Array | Brainlab SE | OLO | 2024-06-04 |
| 04056481144760 | Drill Guide Depth Control (60 - 100 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144777 | Drill Guide Depth Control (0 - 60 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144784 | Drill Guide Tube (4.5 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144791 | Drill Guide Tube (3.2 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144807 | Drill Guide Tube (2.6 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144814 | Drill Guide Tube (2.4 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144821 | Drill Guide Tube (2.0 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481144838 | Drill Guide Handle | Brainlab SE | OLO | 2024-06-04 |
| 04056481145057 | Drill Guide Trocar Insert (2.0 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481145064 | Drill Guide Trocar Insert (2.4 mm) | Brainlab SE | OLO | 2024-06-04 |
| 04056481145071 | Drill Guide Trocar Insert (2.6 mm) | Brainlab SE | OLO | 2024-06-04 |