SR™ MCP

GUDID 00886385021041

SR MCP, IMPLANT, SIZE SMALL

Stryker Trauma SA

Metacarpophalangeal joint prosthesis, one-piece
Primary Device ID00886385021041
NIH Device Record Key546e2e55-8027-4e24-8697-dfdaed1d9ec4
Commercial Distribution StatusIn Commercial Distribution
Brand NameSR™ MCP
Version Model Number5800-SM00
Company DUNS481999654
Company NameStryker Trauma SA
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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx
Phone1-201-831-5000
Emailxx@xx.xx

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness
Special Storage Condition, SpecifyBetween 0 and 0 *Avoid exposure to direct sunlight or dampness

Device Identifiers

Device Issuing AgencyDevice ID
GS100886385021041 [Primary]

FDA Product Code

MPKSemi-Constrained Metal/Polymer Finger Joint Prosthesis

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-10-07
Device Publish Date2017-06-27

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