| Primary Device ID | 40845854061320 |
| NIH Device Record Key | e8111412-9656-403a-b321-cf6516c899da |
| Commercial Distribution Discontinuation | 2023-09-12 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | PLUMEPEN |
| Version Model Number | PROTIP520 |
| Catalog Number | PROTIP520 |
| Company DUNS | 071595540 |
| Company Name | Conmed Corporation |
| Device Count | 20 |
| 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 |
| 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 | |
| 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 | |
| Phone | +1(800)237-0169 |
| CUSTOMER_SERVICE@CONMED.COM |
| 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 Issuing Agency | Device ID |
|---|---|
| GS1 | 00845854061322 [Unit of Use] |
| GS1 | 20845854061326 [Primary] |
| GS1 | 40845854061320 [Package] Contains: 20845854061326 Package: Box [20 Units] Discontinued: 2023-09-12 Not in Commercial Distribution |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
[40845854061320]
Ethylene Oxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2023-09-13 |
| Device Publish Date | 2020-06-06 |
| 20845854061296 | PLP2501 |
| 40845854061320 | PlumePen Pro Disposable Capture Port Tips 5 in (12.7 cm) |
| 00845854084246 | PlumePen Pro, 10ft, PTFE, Non-Sterile, 20/BOX |
| 00845854084239 | PlumePen Pro, 15ft, PTFE, Non-Sterile, 20/BOX |
| 00845854084222 | PlumePen Ultra, 10ft, PTFE, Non-Sterile, 20/BOX |
| 00845854084215 | PlumePen Ultra, 15ft, PTFE, Non-Sterile, 20/BOX |
| 00845854084208 | PlumePen Elite, 10ft, SS, Non-Sterile, 20/BOX |
| 00845854084192 | PlumePen Elite, 10ft, PTFE, Non-Sterile, 20/BOX |
| 00845854084185 | PlumePen Elite, 15ft, PTFE, Non-Sterile, 20/BOX |
| 00845854061308 | PLP2520 |
| 00845854061261 | PLP1020 |
| 40845854061337 | PlumePen Pro Disposable Capture Port Tips 6 in (15.24 cm) |
| 40845854061313 | PlumePen Pro Disposable Capture Port Tips 4 in (10.16 cm) |
| 10845854061305 | PlumePen Elite Surgical Smoke Evacuation Pencil, 7/8" (22 mm), 15 ft. (4.6 m) |
| 10845854061282 | PlumePen Elite Surgical Smoke Evacuation Pencil, 7/8" (22 mm), 10 ft. (3 m) |
| 10845854061268 | PlumePen Elite Surgical Smoke Evacuation Pencil, 7/8" (22 mm), 10 ft. (3 m) |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PLUMEPEN 85076204 4376795 Live/Registered |
Medtek Devices, Inc. 2010-07-01 |