Primary Device ID | H862PS2002 |
NIH Device Record Key | 83255937-6a4d-4442-bcfb-717ade8b4f67 |
Commercial Distribution Discontinuation | 2019-09-11 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Posi-Stick Introducer Set |
Version Model Number | PS2-00 |
Catalog Number | PS2-00 |
Company DUNS | 192559557 |
Company Name | URESIL, LLC |
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 | true |
OTC Over-The-Counter | false |
Phone | 1-800-538-7374 |
sales@uresil.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | H862PS2000 [Primary] |
HIBCC | H862PS2001 [Package] Contains: H862PS2000 Package: Dispenser [10 Units] Discontinued: 2019-09-11 Not in Commercial Distribution |
HIBCC | H862PS2002 [Package] Contains: H862PS2001 Package: Shipper [1 Units] Discontinued: 2019-09-11 Not in Commercial Distribution |
DYB | Introducer, Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-09-12 |
Device Publish Date | 2016-08-29 |
H862PS21S2 | Posi-Stick One-Step |
H862PS21SNC2 | Posi-Stick One-Step |
H862PS238SW2 | Posi-Stick Intro. Set w/PT Marker & .038" Super-Stiff GW |
H862PS2382 | Posi-Stick Intro. Set w/PT Marker & .038" & .018" GW |
H862PS235SW2 | Posi-Stick Intro. Set w/PT Marker & .035" Super-Stiff GW |
H862PS2352 | Posi-Stick Intro. Set w/PT Marker & .035" & .018" GW |
H862PS2182 | Posi-Stick .018" (.046mm) Guidewire |
H862PS2002 | Posi-Stick Introducer Set w/PT Marker |
10817640020506 | Posi-Stick One-Step |