PLUMEPEN PLP2501
GUDID 20845854061296
Conmed Corporation
Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use Open-surgery electrosurgical handpiece/electrode, monopolar, single-use| Primary Device ID | 20845854061296 |
| NIH Device Record Key | d3336ae4-6ed2-417b-aab0-c72fba5969ff |
| Commercial Distribution Discontinuation | 2022-06-08 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | PLUMEPEN |
| Version Model Number | PLP2501 |
| Catalog Number | PLP2501 |
| 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
| 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 |
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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20845854061296 [Primary] |
FDA Product Code
| GEI | Electrosurgical, cutting & coagulation & accessories |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | true |
[20845854061296]
Ethylene Oxide
[20845854061296]
Ethylene Oxide
[20845854061296]
Ethylene Oxide
[20845854061296]
Ethylene Oxide
[20845854061296]
Ethylene Oxide
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-06-09 |
| Device Publish Date | 2020-06-05 |
On-Brand Devices [PLUMEPEN]
| 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) |
Trademark Results [PLUMEPEN]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PLUMEPEN 85076204 4376795 Live/Registered |
Medtek Devices, Inc. 2010-07-01 |
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