Primary Device ID | 07613327376333 |
NIH Device Record Key | ae2b142e-f19c-4147-b21a-4d9876541d36 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 1900010040 |
Catalog Number | 1900010040 |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613327376333 [Primary] |
GFF | BUR, SURGICAL, GENERAL & PLASTIC SURGERY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-24 |
Device Publish Date | 2018-09-23 |
07613327508437 - Tritanium X | 2024-09-16 TL Expandable Curved Posterior Lumbar Cage |
07613327006933 - ES2 SPINAL SYSTEM | 2024-09-11 BLOCKER INSERTER |
07613327006964 - ES2 SPINAL SYSTEM | 2024-09-11 ROD INSERTER |
07613327006995 - ES2 SPINAL SYSTEM | 2024-09-11 RECOVERY GUIDE |
07613327007008 - ES2 SPINAL SYSTEM | 2024-09-11 INNER SHAFT, RECOVERY SYSTEM |
07613327007022 - ES2 SPINAL SYSTEM | 2024-09-11 THREADED RECOVERY GUIDE |
07613327007046 - ES2 SPINAL SYSTEM | 2024-09-11 ROD INSERTER |
07613327114867 - XIA 4.5 EVOLUTION | 2024-09-11 BLOCKER INSERTER |