SR™ MCP

GUDID 00886385020921

S.R. MCP PHALANGEAL BROACH ASSEMBLY, MD

Stryker Trauma SA

Orthopaedic broach

• Primary Device ID: 00886385020921
• NIH Device Record Key: 5f8ffca5-bbb9-4d16-8bd1-3e47b5603abe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SR™ MCP
• Version Model Number: 17-1522
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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

Customer Support Contacts

• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx
• Phone: 1-201-831-5000
• Email: xx@xx.xx

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886385020921 [Primary]

FDA Product Code

• MPK: Semi-Constrained Metal/Polymer Finger Joint Prosthesis

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

[00886385020921]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-06-27

On-Brand Devices [SR™ MCP]

• 00886385021157: SR-MCP Instrument Set
• 00886385021140: SR MCP Instrument Set
• 00886385021102: SR MCP, IMPLANT, SIZE X-SMALL
• 00886385021072: SR MCP, IMPLANT, SIZE X-LARGE
• 00886385021041: SR MCP, IMPLANT, SIZE SMALL
• 00886385021010: SR MCP, IMPLANT, SIZE MEDIUM
• 00886385020983: SR MCP, IMPLANT, SIZE LARGE
• 00886385020976: S.R. MCP INSTRUMENT SET, PHALANGEAL IMPACTOR
• 00886385020969: S.R. MCP INSTRUMENT SET, METACARPAL IMPACTOR
• 00886385020952: S.R. MCP AWL ASSEMBLY, SIZE .062
• 00886385020945: S.R. MCP PHALANGEAL BROACH ASSEMBLY, XL
• 00886385020938: S.R. MCP PHALANGEAL BROACH ASSEMBLY, LG
• 00886385020921: S.R. MCP PHALANGEAL BROACH ASSEMBLY, MD
• 00886385020914: S.R. MCP PHALANGEAL BROACH ASSEMBLY, SM
• 00886385020907: S.R. MCP PHALANGEAL BROACH ASSEMBLY, XS
• 00886385020891: S.R. MCP METACARPAL BROACH, SIZE XL
• 00886385020884: S.R. MCP METACARPAL BROACH, SIZE LG
• 00886385020877: S.R. MCP METACARPAL BROACH, SIZE MD
• 00886385020860: S.R. MCP METACARPAL BROACH, SIZE SM
• 00886385020853: S.R. MCP METACARPAL BROACH, SIZE XS
• 00886385020846: S.R. MCP PHALANGEAL TRIAL, SIZE XL
• 00886385020839: S.R. MCP PHALANGEAL TRIAL, SIZE LG
• 00886385020822: S.R. MCP PHALANGEAL TRIAL, SIZE MD
• 00886385020815: S.R. MCP PHALANGEAL TRIAL, SIZE SM
• 00886385020808: S.R. MCP PHALANGEAL TRIAL, SIZE XS
• 00886385020792: S.R. MCP METACARPAL TRIAL, SIZE XL
• 00886385020785: S.R. MCP METACARPAL TRIAL, SIZE LG
• 00886385020778: S.R. MCP METACARPAL TRIAL, SIZE MD
• 00886385020761: S.R. MCP METACARPAL TRIAL, SIZE SM
• 00886385020754: S.R. MCP METACARPAL TRIAL, SIZE XS
• 00886385020747: Nipple Mat for SR MCP Tray
• 00886385020730: S.R. MCP STERILIZATION TRAY BOTTOM
• 00886385020723: S.R. MCP STERILIZATION TRAY LID
• 00886385020716: S.R. MCP TRIAL EXTRACTOR