Primary Device ID | 07613252574187 |
NIH Device Record Key | bfd93e61-061c-4ca6-9300-73b2cf48679a |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 0306620000 |
Catalog Number | 0306620000 |
Company DUNS | 196548481 |
Company Name | STRYKER 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 | 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 |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com | |
Phone | +1(800)253-3210 |
Inst.Stryker.cs@Stryker.com |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Needle Gauge | 10 Gauge |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613252574187 [Primary] |
OCJ | spinal channeling instrument, vertebroplasty |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-25 |
Device Publish Date | 2018-09-24 |
07613327266849 - MANTIS | 2024-08-01 MANTIS POLY ADJUSTMENT DRIVER |
07613327582949 - Surpass Elite | 2024-07-29 Flow Diverter System |
07613327582994 - Surpass Elite | 2024-07-29 Flow Diverter System |
07613327583021 - Surpass Elite | 2024-07-29 Flow Diverter System |
07613327583106 - Surpass Elite | 2024-07-29 Flow Diverter System |
07613327583113 - Surpass Elite | 2024-07-29 Flow Diverter System |
07613327583120 - Surpass Elite | 2024-07-29 Flow Diverter System |
07613327583137 - Surpass Elite | 2024-07-29 Flow Diverter System |