Primary Device ID | 00814548016412 |
NIH Device Record Key | fda218d7-3171-4762-ad26-3d5f29fdd71a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PX SLIM Delivery Microcatheter |
Version Model Number | PXSLIM045-B |
Company DUNS | 191077671 |
Company Name | PENUMBRA, INC. |
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 | 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814548016412 [Primary] |
DQY | CATHETER, PERCUTANEOUS |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2017-10-02 |
00814548016450 | PXSLIM130 |
00814548016443 | PXSLIMSTR-B |
00814548016436 | PXSLIMSTR-A |
00814548016429 | PXSLIM090 |
00814548016412 | PXSLIM045-B |
00814548016405 | PXSLIM045-A |
00814548012575 | AdvPX400 J 160DualMB |
00814548012568 | AdvPX400 90Deg 160DualMB |
00814548012551 | AdvPX400 45Deg 160DualMB |
00814548012537 | PXSLIM 150Micro, 130Deg |
00814548012520 | PXSLIM 150Micro, 90Deg |
00814548012513 | AdvPX400 45Deg 150DualMB |
00814548012506 | AdvPX400 STR 150DualMB |
00814548010465 | PXSLIM 150Micro, 130Deg |
00814548010342 | PXSLIM 150Micro, 90Deg |