System Drape Kit 1213

GUDID 10841912100658

PROTEK MEDICAL PRODUCTS, INC.

Instrument/equipment drape, single-use, sterile

• Primary Device ID: 10841912100658
• NIH Device Record Key: 72d4b4a0-6a40-48fe-a1b7-60b9d03b9523
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: System Drape Kit
• Version Model Number: 1213
• Catalog Number: 1213
• Company DUNS: 965417181
• Company Name: PROTEK MEDICAL PRODUCTS, INC.
• 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: 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841912100651 [Primary]
GS1	10841912100658 [Package]; Contains: 00841912100651; Package: [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970885

FDA Product Code

• MMP: Cover, Barrier, Protective

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-16

On-Brand Devices [System Drape Kit]

• 10841912100658: 1213
• 10841912100641: 1212