Rampart M1128-ODK

GUDID 17466532979229

Rampart OUS Drape Kit

DAS Medical International SRL

Medical equipment drape, single-use

• Primary Device ID: 17466532979229
• NIH Device Record Key: 965f4442-f635-42d8-87f7-e13eb2b177de
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rampart
• Version Model Number: M1128-ODK
• Catalog Number: M1128-ODK
• Company DUNS: 817435655
• Company Name: DAS Medical International SRL
• Device Count: 1
• 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: true
• 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: true

Customer Support Contacts

• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx
• Phone: 809-556-8900
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07466532979222 [Primary]
GS1	17466532979229 [Package]; Contains: 07466532979222; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• PUI: Drape, Surgical, Exempt

Sterilization

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

[17466532979229]

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Ethylene Oxide

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Ethylene Oxide

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-04-15
• Device Publish Date: 2021-04-07

On-Brand Devices [Rampart]

• 17466532979229: Rampart OUS Drape Kit
• 17467423230528: Rampart M1130 Drape (M1130- CDK)
• 27466532979325: RAMPART M1128 DRAPE KIT (M1128-CDK)