Primary Device ID | 04546540132253 |
NIH Device Record Key | c1b54771-5d8b-4b04-9d10-a6f2741098ef |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 0940023000 |
Catalog Number | 0940023000 |
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 |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Width | 63.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540132253 [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 |
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