Primary Device ID | 20653405986468 |
NIH Device Record Key | 593deb22-040d-4380-b8ef-efd9f737de5b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BEAMER |
Version Model Number | S-BEAM-3 |
Catalog Number | S-BEAM-3 |
Company DUNS | 071595540 |
Company Name | Conmed Corporation |
Device Count | 10 |
DM Exempt | true |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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 |
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 | 00653405986464 [Unit of Use] |
GS1 | 10653405986461 [Primary] |
GS1 | 20653405986468 [Package] Contains: 10653405986461 Package: BOX [10 Units] In Commercial Distribution |
GEI | Electrosurgical, cutting & coagulation & accessories |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2019-04-15 |
10653405064206 | BEAMER ARGON SNARE PROBE |
10653405064190 | BEAMER ARGON SNARE PROBE |
10653405064183 | BEAMER ARGON SNARE PROBE |
10653405064176 | BEAMER ARGON SNARE PROBE |
10653405064169 | BEAMER ARGON SNARE PROBE |
20653405986468 | BEAMER ARGON SIDEFIRE PROBE, SIDEFIRE PROBE FOR FLEXIBLE ENDOSCOPY |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BEAMER 97921883 not registered Live/Pending |
SOFTORINO INC. 2023-05-05 |
BEAMER 88924661 not registered Live/Pending |
Conmed Corporation 2020-05-20 |
BEAMER 88730471 not registered Live/Pending |
ARCH Cutting Tools Corp. 2019-12-17 |
BEAMER 88602347 not registered Live/Pending |
Rodney Kuznicki 2019-09-03 |
BEAMER 87645376 5433559 Live/Registered |
Discount Tobacco Products, Inc. 2017-10-13 |
BEAMER 87643707 5613309 Live/Registered |
Discount Tobacco Products, Inc. 2017-10-12 |
BEAMER 87643673 5613308 Live/Registered |
Discount Tobacco Products, Inc. 2017-10-12 |
BEAMER 87643620 not registered Live/Pending |
Discount Tobacco Products, Inc. 2017-10-12 |
BEAMER 87643584 5613306 Live/Registered |
Discount Tobacco Products, Inc. 2017-10-12 |
BEAMER 86859198 5026003 Live/Registered |
Hazelden Betty Ford Foundation 2015-12-28 |
BEAMER 86824987 4932612 Live/Registered |
Hazelden Betty Ford Foundation 2015-11-18 |
BEAMER 86189975 4740251 Live/Registered |
Discount Tobacco Products, Inc. 2014-02-11 |