PATHWAY 950501611

GUDID 10603295227144

PATHWAY QUICK DRILL PIN MI

DEPUY INTERNATIONAL LTD

Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable Orthopaedic bone pin, non-bioabsorbable

• Primary Device ID: 10603295227144
• NIH Device Record Key: aba0d85e-d633-4560-9a19-f62ecc0b58b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PATHWAY
• Version Model Number: 9505-01-611
• Catalog Number: 950501611
• Company DUNS: 896498813
• Company Name: DEPUY INTERNATIONAL LTD
• Device Count: 1
• DM Exempt: true
• 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10603295227144 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

[10603295227144]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-05-13
• Device Publish Date: 2018-09-24

On-Brand Devices [PATHWAY]

• 10603295226499: M.B.T. PATHWAY BUSHING EXTRACTOR
• 10603295227144: PATHWAY QUICK DRILL PIN MI
• 10603295227113: PATHWAY TIBIAL/FEMORAL RM/LL 0 DEGREE
• 10603295227090: PATHWAY TIBIAL/FEMORAL LM/RL 0 DEGREE
• 10603295226956: PATHWAY FEMORAL BOW YOKE
• 10603295226949: M.B.T. PATHWAY NON-CEMENTED KEEL PUNCH BUSHING SIZE 4-7
• 10603295226932: M.B.T. PATHWAY NON-CEMENTED KEEL PUNCH BUSHING SIZE 2-3
• 10603295226925: M.B.T. PATHWAY NON-CEMENTED KEEL PUNCH BUSHING SIZE 1-1.5
• 10603295226529: M.B.T. PATHWAY KEEL PUNCH BUSHING SIZE 4-7
• 10603295226512: M.B.T. PATHWAY KEEL PUNCH BUSHING SIZE 2-3
• 10603295226505: M.B.T. PATHWAY KEEL PUNCH BUSHING SIZE 1-1.5
• 10603295226444: M.B.T. PATHWAY TIBIAL TEMPLATE SIZE 4.5
• 10603295224808: PATHWAY TIBIAL STYLUS
• 10603295026969: PATHWAY TIBIAL SCREW 21mm