| Primary Device ID | 10653405048367 |
| NIH Device Record Key | 3211bd27-9d03-4f4f-b04b-d69cd5e26f93 |
| Commercial Distribution Discontinuation | 2022-02-02 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | PadPro |
| Version Model Number | 1400 |
| Catalog Number | 1400 |
| 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10653405048367 [Primary] |
| MKJ | Automated external defibrillators (non-wearable) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2022-02-04 |
| Device Publish Date | 2016-10-07 |
| 00653405056198 | ZOLL SHORT |
| 00653405056181 | HP Short |
| 00653405056174 | HS-XL PIG |
| 00653405055771 | DT 2200 |
| 00653405054880 | QUICK SHORT |
| 00653405048377 | ZOLL PIG |
| 00653405048360 | 1400 |
| 00653405046960 | 1200 |
| 00653405046953 | 1105 |
| 00653405046946 | LP-10 |
| 00653405046939 | LP9-8 |
| 00653405046922 | M3508A |
| 00653405046915 | M3507A |
| 00653405046892 | EXT10 |
| 00653405046885 | 1750B |
| 00653405046878 | 1750A |
| 00653405046861 | LP-12 |
| 00653405046854 | QUICK PIG |
| 00653405046847 | HP PIG |
| 00653405046830 | LP-500 |
| 00653405046823 | HS-XL |
| 00653405046816 | SHRTG BLOCK |
| 00653405040173 | HP4R |
| 00653405040166 | HP |
| 00653405040159 | ZOLL |
| 00653405040142 | R2 |
| 00653405040135 | QUICK |
| 20653405077630 | 2602H |
| 20653405076985 | 2001H-PC |
| 20653405065354 | 2516H-PC |
| 20653405064296 | 2001H-C |
| 10653405064282 | 2001H |
| 20653405064272 | 2001R |
| 20653405064265 | 2603H |
| 20653405064258 | 2516H |
| 20653405064241 | 2603R |
| 20653405064234 | 2516R |
| 20653405042751 | 2603P |
| 20653405042744 | 2602P |
| 10653405042730 | 2516P-PC |
| 20653405042720 | 2516P |
| 20653405042713 | 2502P |
| 20653405042690 | 2001P-PC |
| 20653405042683 | 2001P-C |
| 20653405042676 | 2001P |
| 20653405042652 | 2603M |
| 20653405042645 | 2602M |
| 20653405042638 | 2516M-PC |
| 20653405042621 | 2516M |
| 20653405042614 | 2502M |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() PADPRO 85759127 4350138 Live/Registered |
Flow Data, Inc. 2012-10-19 |
![]() PADPRO 78314688 2905049 Live/Registered |
ConMed Corporation 2003-10-16 |
![]() PADPRO 78103715 not registered Dead/Abandoned |
PADPRO LLC 2002-01-19 |