| Primary Device ID | 05391529584566 |
| NIH Device Record Key | 7e7e6e41-4233-4166-b8ec-7e48f9a80302 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Apex |
| Version Model Number | T02-100360 |
| Catalog Number | T02-100360 |
| Company DUNS | 985596830 |
| Company Name | ORTHOXEL DESIGNATED ACTIVITY COMPANY |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Special Storage Condition, Specify | Between 0 and 0 *Ambient Storage and Handling |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05391529584566 [Primary] |
| HSB | Rod, Fixation, Intramedullary And Accessories |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-02-15 |
| Device Publish Date | 2021-02-05 |
| 05391529580797 | Apex Tibial Endcap |
| 05391529580780 | Apex Tibia Endcap |
| 05391529580773 | Apex Tibial Endcap |
| 05391529580582 | Apex Tibial Nail, Sterile |
| 05391529580193 | Apex Tibia Screw, Sterile |
| 05391529580186 | Apex Tibial Screw, Sterile |
| 05391529580179 | Apex Tibial Screw, Sterile |
| 05391529580162 | Apex Tibial Screw, Sterile |
| 05391529580155 | Apex Tibial Screw, Sterile |
| 05391529580148 | Apex Tibial Screw, Sterile |
| 05391529582180 | Tibial Extraction Bolt |
| 05391529581459 | Tibial Insertion Handle |
| 05391529581237 | Tibial Radiolucent Guide ML |
| 05391529581114 | Tibial Insertion Bolt |
| 05391529585150 | Apex Tibial Nailing System Case |
| 05391529584245 | Yellow Ø4.25mm Drill Sleeve (Length 138.5mm) |
| 05391529584238 | Trocar Ø8.0mm x Length 150.0mm |
| 05391529584221 | Green Outer Drill Sleeve (Length 129mm) |
| 05391529584214 | Suprapatellar AO Mount Anchor Pin |
| 05391529584207 | AO Mount Drill Extension (Length 136.5mm) |
| 05391529584191 | Suprapatellar Trocar |
| 05391529584184 | Suprapatellar K-Wire Guide |
| 05391529584177 | Suprapatellar Standard Protection Sleeve |
| 05391529584160 | Suprapatellar Anchoring Protection Sleeve |
| 05391529584153 | Suprapatellar Protection Sleeve Handle Connector |
| 05391529584146 | Suprapatellar Protection Sleeve Handle |
| 05391529584139 | Tibial Suprapatellar Connecting Bolt |
| 05391529584122 | Tibial Suprapatellar Insert Retainer |
| 05391529584115 | Tibial Infrapatellar Connecting Bolt |
| 05391529584108 | Tibial Infrapatellar Insert Retainer |
| 05391529584092 | Tibial Targeting Guide Locking Bolt |
| 05391529584085 | Tibial Targeting Guide |
| 05391529584078 | Tibial Suprapatellar Insertion Handle |
| 05391529584061 | Tibial Infrapatellar Insertion Handle |
| 05391529584054 | Ø12 Cannulated Curved Awl |
| 05391529583149 | Large AO T-Handle |
| 05391529583125 | Insert Retainer Containing Bolt |
| 05391529583101 | Monobloc Reamer, Size 8.0 |
| 05391529583095 | Yellow Ø4.25mm Twist Drill X Length 300mm (Use Ø5.00mm Locking Screw) |
| 05391529583088 | Monobloc Reamer, Size 7.0 |
| 05391529583071 | Locking Screw Length Gauge (Hook) |
| 05391529583064 | Monobloc Reamer, Size 6.0 |
| 05391529583057 | Flexible IM reamer Shaft 470mm |
| 05391529583040 | Modular Reamer Head, Size 16.0 |
| 05391529583033 | Modular Reamer Head, Size 15.5 |
| 05391529583026 | Modular Reamer Head, Size 15.0 |
| 05391529583019 | Modular Reamer Head, Size 14.5 |
| 05391529583002 | Modular Reamer Head, Size 14.0 |
| 05391529582999 | Modular Reamer Head, Size 13.5 |
| 05391529582982 | Modular Reamer Head, Size 13.0 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() APEX 98811987 not registered Live/Pending |
AFTERMARKET PERFORMANCE EXPRESS 2024-10-21 |
![]() APEX 98805060 not registered Live/Pending |
Dongguan Luxshare Technology Co., Ltd. 2024-10-16 |
![]() APEX 98733536 not registered Live/Pending |
Apex natural nutrition inc. 2024-09-04 |
![]() APEX 98674096 not registered Live/Pending |
Medtronic Xomed, Inc. 2024-07-30 |
![]() APEX 98673954 not registered Live/Pending |
Covert Instruments LLC 2024-07-30 |
![]() APEX 98668271 not registered Live/Pending |
Smith-Root, Inc. 2024-07-26 |
![]() APEX 98662611 not registered Live/Pending |
FRC Global Inc. 2024-07-23 |
![]() APEX 98644654 not registered Live/Pending |
Blume, Phillip James 2024-07-11 |
![]() APEX 98636442 not registered Live/Pending |
Catalina Carpet Mills Inc. 2024-07-08 |
![]() APEX 98616917 not registered Live/Pending |
Lander Hospitality Holdings LLC 2024-06-25 |
![]() APEX 98616917 not registered Live/Pending |
Hines, Victor Nunzio 2024-06-25 |
![]() APEX 98616917 not registered Live/Pending |
Comes, Bryan 2024-06-25 |