MAC 675023

GUDID 07613327261820

SCREWDRIVER

Stryker Corporation

Surgical screwdriver, reusable

• Primary Device ID: 07613327261820
• NIH Device Record Key: 8804aced-0995-4f73-b3ac-ed768ac12e1c
• Commercial Distribution Discontinuation: 2024-11-08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MAC
• Version Model Number: 675023
• Catalog Number: 675023
• Company DUNS: 149183167
• 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: true
• 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

Device Dimensions

• 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 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 Identifiers

Device Issuing Agency	Device ID
GS1	07613327261820 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

[07613327261820]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2024-10-29
• Device Publish Date: 2019-11-25

Devices Manufactured by Stryker Corporation

• 07613327261844 - O.I.C. TITANIUM: 2026-02-09 CAGE IMPACTOR
• 07613327261868 - O.I.C. TITANIUM: 2026-02-09 FINAL CAGE IMPACTOR
• 07613327264722 - XIA 4.5: 2026-02-09 HOOK IMPACTOR
• 07613327264753 - XIA 4.5: 2026-02-09 DUAL STAPLE IMPACTOR
• 07613327265460 - XIA 3: 2026-02-09 HOOK IMPACTOR
• 07613327267037 - VLIFT: 2026-02-09 ENDCAP IMPACTOR
• 07613327267068 - VLIFT: 2026-02-09 ENDCAP IMPACTOR
• 07613327267563 - AVS: 2026-02-09 AS SPACER IMPACTOR STRAIGHT