DRAPE

GUDID 00840186699946

DRP1000A Size Customized (GREY VINYL DRAPE ABOVE TABLE ATTACHMENT), 5mm Regular Lead

BURLINGTON MEDICAL, LLC

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• Primary Device ID: 00840186699946
• NIH Device Record Key: b8f1de9a-1d89-4b0f-b778-def9e9bc04b5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRAPE
• Version Model Number: DRP1000A-C
• Company DUNS: 083381202
• Company Name: BURLINGTON MEDICAL, LLC
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840186699946 [Primary]

FDA Product Code

• EAK: Screen, Leaded, Operator Radiation Protector

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-30
• Device Publish Date: 2022-09-22

On-Brand Devices [DRAPE]

• 00840186698178: DRAPE (DRAPE) Tailored, .5mm Regular Lead
• 00840186699946: DRP1000A Size Customized (GREY VINYL DRAPE ABOVE TABLE ATTACHMENT), 5mm Regular Lead
• 00840186699939: DRP1000A (GREY VINYL DRAPE ABOVE TABLE ATTACHMENT), 5mm Regular Lead
• 00840186698215: DRP2000 DRAPE-C (DRAPE ONLY-CUSTOM DOUBLE PIVOT), .5mm Regular Lead
• 00840186698208: DRP2000 DRAPE (DRAPE ONLY GREY VINYL DOUBLE PIVOT), .5mm Regular Lead
• 00840186698192: DRP1000 DRAPE-C (DRAPE ONLY-CUSTOM SINGLE PIVOT), .5mm Regular Lead
• 00840186698185: DRP1000 DRAPE (DRAPE ONLY-GREY VINYL SINGLE PIVOT), .5mm Regular Lead