AO 4100-210-000S1

GUDID 07613154055180

Large Reamer

STRYKER CORPORATION

Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck Surgical drill chuck
Primary Device ID07613154055180
NIH Device Record Keyeec6a7a6-f5df-467e-9614-957cd30627f0
Commercial Distribution StatusIn Commercial Distribution
Brand NameAO
Version Model Number4100210000S1
Catalog Number4100-210-000S1
Company DUNS196548481
Company NameSTRYKER CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107613154055180 [Primary]

FDA Product Code

HRXARTHROSCOPE

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


[07613154055180]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number8
Public Version Date2019-11-22
Device Publish Date2017-02-23

On-Brand Devices [AO]

07613327115123Right Angle Drive - Large Reamer
07613154055180Large Reamer
04546540501707Large Reamer
04546540501615Small Drill
045465402164723.25:1 Large Reamer
045465402164031:1 Small Drill
04546540068217Large Reamer
04546540068156Small Drill

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.