SurgiLock SLS1007

GUDID 00850047863041

Safety Instrument Platform, 10" X 7", Sterile

Medicalock Corporation

General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use General surgical procedure kit, non-medicated, single-use

• Primary Device ID: 00850047863041
• NIH Device Record Key: ab8d064a-6702-4d04-8590-415929ed4728
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SurgiLock
• Version Model Number: SLS1007
• Catalog Number: SLS1007
• Company DUNS: 118863171
• Company Name: Medicalock Corporation
• Device Count: 15
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 6084302475
• Email: jodie@medicalock.com
• Phone: 6084302475
• Email: jodie@medicalock.com
• Phone: 6084302475
• Email: jodie@medicalock.com
• Phone: 6084302475
• Email: jodie@medicalock.com
• Phone: 6084302475
• Email: jodie@medicalock.com
• Phone: 6084302475
• Email: jodie@medicalock.com
• Phone: 6084302475
• Email: jodie@medicalock.com

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 Identifiers

Device Issuing Agency	Device ID
GS1	00850047863041 [Unit of Use]
GS1	00850047863058 [Primary]

FDA Product Code

• PUI: Drape, Surgical, Exempt

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-15
• Device Publish Date: 2024-04-05

On-Brand Devices [SurgiLock]

• 00850047863041: Safety Instrument Platform, 10" X 7", Sterile
• 00850047863010: Safety Instrument Platform, 10" X 16", Sterile