Cortina
- Primary DI
- 00841508105794
- Brand
- Cortina
- Company
- NEUROSTRUCTURES, INC
- Model
- 31-90-006-28090900
- Device description
- Trials 28x9x9x0
- Published
- 2016-01-11
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
Contact Domains#
Product Codes#
| Code | Name |
|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Product Code Classifications#
| Code | Device | Specialty | Class |
|---|---|---|---|
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar | Orthopedic | 2 |
Identifiers And Packaging#
| Identifier | Type | Agency | Package quantity | Status |
|---|---|---|---|---|
| 00841508105794 | Primary | GS1 | 0 |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|---|---|---|
| 00841508105794 | 00841508105794 | 841508105794 | 0841508105794 |
GMDN Terms#
| Term | Definition |
|---|---|
| General internal orthopaedic fixation system implantation kit | A collection of instruments and devices intended to be used for the placement of an internal orthopaedic fixation system into or onto all types of bones (e.g., bones of limbs, spine, pelvis, or craniomaxillofacial). It is a non-dedicated device that includes various metallic and/or plastic reusable devices [e.g., retractors, rods, clamps, drills, pins, saws, screwdrivers, guides, trials, impactors] intended to be used for the implantation of any type of internal orthopaedic fixation system; the implant(s) is not included. This is a reusable device. |
Sterilization Methods#
| Method |
|---|
| Moist Heat or Steam Sterilization |
Contacts#
| Phone | |
|---|---|
| 8003526103 | customerservice@neurostructures.com |
Regulatory Flags#
- DUNS number
- 079391677
- Device count
- 1
- DM exempt
- true
- Lot or batch
- true
- Sterilization required before use
- true
Other Devices From This Company#
| Primary DI | Brand | Model | Catalog | Published |
|---|---|---|---|---|
| 00841508100003 | Tempus™ | 10-01-012 | 2016-03-09 | |
| 00841508100010 | Tempus™ | 10-01-014 | 2015-09-17 | |
| 00841508100027 | Tempus™ | 10-01-016 | 2015-09-17 | |
| 00841508100034 | Tempus™ | 10-01-018 | 2015-09-17 | |
| 00841508100041 | Tempus™ | 10-01-020 | 2015-09-17 | |
| 00841508100058 | Tempus™ | 10-01-022 | 2015-09-17 | |
| 00841508100065 | Tempus™ | 10-01-024 | 2015-09-17 | |
| 00841508100072 | Tempus™ | 10-01-026 | 2015-09-17 | |
| 00841508100089 | Tempus™ | 10-02-024 | 2015-09-17 | |
| 00841508100096 | Tempus™ | 10-02-026 | 2015-09-17 | |
| 00841508100102 | Tempus™ | 10-02-028 | 2015-09-17 | |
| 00841508100119 | Tempus™ | 10-02-030 | 2015-09-17 | |
| 00841508100126 | Tempus™ | 10-02-032 | 2015-09-17 | |
| 00841508100133 | Tempus™ | 10-02-034 | 2015-09-17 | |
| 00841508100140 | Tempus™ | 10-02-037 | 2015-09-17 | |
| 00841508100157 | Tempus™ | 10-02-040 | 2015-09-17 | |
| 00841508100164 | Tempus™ | 10-02-043 | 2015-09-17 | |
| 00841508100171 | Tempus™ | 10-02-046 | 2015-09-17 | |
| 00841508100188 | Tempus™ | 10-03-039 | 2015-09-17 | |
| 00841508100195 | Tempus™ | 10-03-042 | 2015-09-17 |
Other Devices Sharing Product Codes#
| Primary DI | Brand | Company | Product code | Published |
|---|---|---|---|---|
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| 00841523178896 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. | MAX | 2026-05-22 |
| 00841523178902 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. | MAX | 2026-05-22 |
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| 00841523178926 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. | MAX | 2026-05-22 |
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| 00841523178940 | Kyocera Medical Technologies, Inc. | KYOCERA MEDICAL TECHNOLOGIES, INC. | MAX | 2026-05-22 |
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