Primary Device ID | 04546540130358 |
NIH Device Record Key | 44c351c8-f0e7-47c6-8a01-b313c73b2ec2 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 0840040250 |
Catalog Number | 0840040250 |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | 04546540130358 [Primary] |
LGH | INSTRUMENT, CAST REMOVAL, AC-POWERED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-24 |
Device Publish Date | 2018-09-23 |
07613327625158 - Steri-Shield | 2025-03-03 8 Charger |
37613327625173 - Steri-Shield | 2025-03-03 8 Hood, Standard |
37613327625180 - Steri-Shield | 2025-03-03 8 Hood with Peel Away Face Shield |
37613327625197 - Steri-Shield | 2025-03-03 8 Pullover Toga with Peel Away Face Shield |
37613327625210 - Steri-Shield | 2025-03-03 8 Pullover Toga with Peel Away Face Shield |
37613327625227 - Steri-Shield | 2025-03-03 8 Pullover Toga with Peel Away Face Shield |
37613327625234 - Steri-Shield | 2025-03-03 8 Hood with Anti-Reflective Face Shield |
37613327625241 - Steri-Shield | 2025-03-03 8 Pullover Toga with Peel Away Face Shield |