Primary Device ID | 00841492102083 |
NIH Device Record Key | e6d465a5-7174-4f23-a398-b6095f8b846a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Responder |
Version Model Number | R5KANN |
Company DUNS | 005105515 |
Company Name | RAULAND-BORG CORPORATION |
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 | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841492102083 [Primary] |
OUG | Medical Device Data System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-06-02 |
Device Publish Date | 2017-11-21 |
00841492104681 | 354017 |
00841492104490 | 354001 |
00841492104476 | 354000 |
00841492104438 | 353100 |
00841492104384 | 353001 |
00841492104308 | 352000 |
00841492104285 | 351310 |
00841492104186 | 351004 |
00841492103899 | 3225300 |
00841492102526 | R5KUCNL |
00841492102441 | R5KPS1A |
00841492102175 | R5KDC016 |
00841492102083 | R5KANN |
00841492101949 | R4K12A |
00841492101932 | R4K11V |
00841492101833 | R4KSS |
00841492101826 | R4KSR1 |
00841492101819 | R4KSPK |
00841492101789 | R4KSAR |
00841492101680 | R4KPC10 |
00841492101666 | R4KPB23 |
00841492101352 | R4KANNV2 |
00841492101116 | NCUS1 |
00841492100881 | NCLCD |
00841492100829 | NCDUTY |
00841492100416 | DCV100 |
00841492100232 | CLA246 |
00841492102496 | R5KSMST |
00841492102090 | R5KAUDPC |