NUMATRIX 901201
GUDID 10845854080658
CONMED MIXING AND DELIVERY KIT
Conmed Corporation
Arthroscopic surgical procedure kit, non-medicated, single-use| Primary Device ID | 10845854080658 |
| NIH Device Record Key | 5b7a0064-d852-43f7-bb07-8f85a9a9f8a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | NUMATRIX |
| Version Model Number | 901201 |
| Catalog Number | 901201 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Operating and Storage Conditions
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
| Special Storage Condition, Specify | Between 0 and 0 *KEEP DRY |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10845854080658 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K142535
FDA Product Code
| FMF | Syringe, piston |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
[10845854080658]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2023-06-19 |
| Device Publish Date | 2016-09-24 |
Devices Manufactured by Conmed Corporation
| 10653405008125 - NA | 2024-12-04 CONMED REUSABLE DISPERSIVE ELECTRODE |
| 10653405008132 - NA | 2024-12-04 CONMED REUSABLE PEDIATRIC DISPERSIVE ELECTRODE |
| 30653405987585 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz |
| 30653405987592 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz |
| 30653405987608 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit, 220V-240V 50/60 Hz |
| 30653405990141 - PlumeSafe® X5™ | 2024-10-22 PlumeSafe® X5™ Smoke Evacuation Unit with PlumeSafe® X5™ Smoke Evacuator Filter, 220V-240V 50/60 Hz |
| 20653405990120 - BioBrace | 2024-09-30 BioBrace® Reinforced Implant, 23 x 25 mm |
| 20653405990137 - BioBrace | 2024-09-30 BioBrace® Reinforced Implant, 35 x 25 mm |
Trademark Results [NUMATRIX]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 NUMATRIX 86055223 not registered Dead/Abandoned |
Musculoskeletal Transplant Foundation 2013-09-04 |
 NUMATRIX 77802713 not registered Dead/Abandoned |
Musculoskeletal Transplant Foundation 2009-08-12 |
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