DRLP Drill Guide Block, Standard, Left MDS140908SL

GUDID 10812269021002

DRLP Drill Guide Block, Standard, Left

MIAMI DEVICE SOLUTIONS LLC

Orthopaedic implant aiming/guiding block, reusable

• Primary Device ID: 10812269021002
• NIH Device Record Key: 778106eb-14b3-4b75-a325-40824ba2e6c6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRLP Drill Guide Block, Standard, Left
• Version Model Number: MDS140908SL
• Catalog Number: MDS140908SL
• Company DUNS: 078703080
• Company Name: MIAMI DEVICE SOLUTIONS LLC
• 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: 786-422-1400
• Email: customerservice@miamidevicesolutions.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10812269021002 [Primary]

FDA Product Code

• HWC: Screw, Fixation, Bone

Sterilization

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

[10812269021002]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-05-13
• Device Publish Date: 2019-05-03

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