| Primary Device ID | 30845854027145 |
| NIH Device Record Key | 88dfd681-012d-4d58-9fa3-655a59175cf0 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | HD5544 |
| Catalog Number | HD5544 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| 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 |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 45 degree |
| Outer Diameter | 5.5 Millimeter |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854027148 [Primary] |
| GS1 | 30845854027145 [Direct Marking] |
| GCJ | Laparoscope, general & plastic surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
[30845854027145]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 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 |