Rampart M1128-ODK

GUDID 17466532979229

Rampart OUS Drape Kit

DAS Medical International SRL

Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use Medical equipment drape, single-use 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

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]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

Ethylene Oxide

[17466532979229]

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

Devices Manufactured by DAS Medical International SRL

• 17466532979236 - Asensus: 2021-05-18 Senhance Articulating Drape (X9007762)
• 17466532979243 - Asensus: 2021-05-18 Senhance USB-C LIA Drape (X9007763)
• 17466532979113 - Schaerer: 2021-05-11 Urology Drain Bag
• 17466532979137 - Schaerer: 2021-05-11 Patient Isolation Drape
• 17466532979144 - Proteger: 2021-05-11 Zeiss 65D Surgical Protection System 53" X 120" (ZP6553120)
• 17466532979175 - Proteger: 2021-05-11 Leica 68D Surgical Protection System 53" X 120" (LP6853120)
• 17466532979229 - Rampart: 2021-04-15Rampart OUS Drape Kit
• 17466532979229 - Rampart: 2021-04-15 Rampart OUS Drape Kit
• 07466532979017 - TransEnterix: 2021-03-29 Senhance Manipulator Drape 1-PK X9007635