PlumePort BLAP100
GUDID 10851136002430
Laparoscopic Smoke Filtration Device
Buffalo Filter
Surgical plume evacuation system tube| Primary Device ID | 10851136002430 |
| NIH Device Record Key | 553f0aa1-41ee-40fb-9e72-9bebb209bc05 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PlumePort |
| Version Model Number | SE |
| Catalog Number | BLAP100 |
| Company DUNS | 787855907 |
| Company Name | Buffalo Filter |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00851136002433 [Primary] |
| GS1 | 10851136002430 [Package] Contains: 00851136002433 Package: case [12 Units] In Commercial Distribution |
FDA Product Code
| NKC | Tubing/Tubing With Filter, Insufflation, Laparoscopic |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-01-13 |
On-Brand Devices [PlumePort]
| 10815198012028 | Laparoscopic Plume Filtration Device |
| 10851136002584 | Laparoscopic Smoke Filtration Device |
| 10851136002430 | Laparoscopic Smoke Filtration Device |
| 10851136002423 | Laparoscopic Smoke Filtration Device |
Trademark Results [PlumePort]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PLUMEPORT 86338651 4798109 Live/Registered |
Buffalo Filter LLC 2014-07-16 |
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