Primary Device ID | 00850044399239 |
NIH Device Record Key | 7532fb61-1645-43ae-8b0a-09db7f60a06f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NES Reprocessed .035 Stryker Catheter |
Version Model Number | R-S88901 |
Catalog Number | R-S88901 |
Company DUNS | 608625823 |
Company Name | NORTH EAST SCIENTIFIC INC |
Device Count | 1 |
DM Exempt | true |
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 | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com | |
Phone | 203-756-2111 |
sales@nescientific.com |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Catheter Working Length | 90 Centimeter |
Lumen/Inner Diameter | 0.035 Inch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850044399239 [Primary] |
HIBCC | B227RS889011 [Previous] |
OWQ | Reprocessed Intravascular Ultrasound Catheter |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-05-29 |
Device Publish Date | 2025-05-21 |
B227RS889011 | NES Reprocessed .035 IVUS reprocessed for Stryker (SSS) |
00850044399239 | NES Reprocessed .035 IVUS reprocessed for Stryker (SSS) |