Primary Device ID | 00811311020379 |
NIH Device Record Key | 4909c47b-d00b-4c99-a89f-08a6d69ff184 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ENROUTE Transcarotid Stent |
Version Model Number | SR-0530-CS |
Catalog Number | SR-0530-CS |
Company DUNS | 022516829 |
Company Name | SILK ROAD MEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00811311020379 [Primary] |
NIM | Stent, Carotid |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-17 |
Device Publish Date | 2016-07-28 |
00811311020539 | 10 mm X 40 mm |
00811311020522 | 10 mm X 30 mm |
00811311020515 | 10 mm X 20 mm |
00811311020508 | 9 mm X 40 mm |
00811311020492 | 9 mm X 30 mm |
00811311020485 | 9 mm X 20 mm |
00811311020478 | 8 mm X 40 mm |
00811311020461 | 8 mm X 30 mm |
00811311020454 | 8 mm X 20 mm |
00811311020447 | 7 mm X 40 mm |
00811311020430 | 7 mm X 30 mm |
00811311020423 | 7 mm X 20 mm |
00811311020416 | 6 mm X 40 mm |
00811311020409 | 6 mm X 30 mm |
00811311020393 | 6 mm X 20 mm |
00811311020386 | 5 mm X 40 mm |
00811311020379 | 5 mm X 30 mm |
00811311020362 | 5 mm X 20 mm |
00811311021321 | 10-7mm x 40mm |
00811311021314 | 10-8mm x 40mm |
00811311021307 | 10-8mm x 30mm |
00811311021291 | 9-7mm x 40mm |
00811311021284 | 9-7mm x 30mm |
00811311021277 | 8-6mm x 40mm |
00811311021260 | 8-6mm x 30mm |