Guide Pin - 3.2 mm Dia LH Threaded Tip

GUDID 00810055521951

Guide Pin - 3.2 mm Dia LH Threaded Tip

Si-Bone Inc.

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: 00810055521951
• NIH Device Record Key: 5da7cb83-b962-46b7-a7c1-5521d5ffc902
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Guide Pin - 3.2 mm Dia LH Threaded Tip
• Version Model Number: 501385
• Company DUNS: 830127168
• Company Name: Si-Bone Inc.
• 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: true
• 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: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com
• Phone: 855-884-3873
• Email: info@si-bone.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810055521951 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

[00810055521951]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-09-18
• Device Publish Date: 2022-12-08

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