PHLP Drill Guide Block, Right MDS130904R

GUDID 10812269021149

PHLP Drill Guide Block, Right

MIAMI DEVICE SOLUTIONS LLC

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 10812269021149
• NIH Device Record Key: dc51ea8b-8236-4198-bded-d689d22dae3a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PHLP Drill Guide Block, Right
• Version Model Number: MDS130904R
• Catalog Number: MDS130904R
• 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	10812269021149 [Primary]

FDA Product Code

• HRS: Plate, Fixation, Bone

Sterilization

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

[10812269021149]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2020-04-06
• Device Publish Date: 2020-02-26

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