| Primary Device ID | 30845854027138 |
| NIH Device Record Key | 4dd2ba98-5f4e-4e00-9e5b-1641fce78afc |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | HD5531 |
| Catalog Number | HD5531 |
| 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 |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| Outer Diameter | 5.5 Millimeter |
| Angle | 30 degree |
| 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 | 20845854027131 [Primary] |
| GS1 | 30845854027138 [Direct Marking] |
| GCJ | Laparoscope, general & plastic surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
Moist Heat or Steam Sterilization
[30845854027138]
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 |
| 30653405990486 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 15MM, TITANIUM |
| 30653405990493 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 6MM X 20MM, TITANIUM |
| 30653405990509 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 15MM, TITANIUM |
| 30653405990516 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 20MM, TITANIUM |
| 30653405990523 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 7MM X 30MM, TITANIUM |
| 30653405990530 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 15MM, TITANIUM |
| 30653405990547 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 20MM, TITANIUM |
| 30653405990554 - EZSTART | 2025-05-21 EZSTART INTERFERENCE SCREW, 8MM X 25MM, TITANIUM |