PullUp Surgical Probe Cover Kit 2002EUR

GUDID 00841912100095

PROTEK MEDICAL PRODUCTS, INC.

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• Primary Device ID: 00841912100095
• NIH Device Record Key: 7d4f9afb-5884-4f5c-9b3b-3708d922866e
• Commercial Distribution Discontinuation: 2020-02-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: PullUp Surgical Probe Cover Kit
• Version Model Number: 2002
• Catalog Number: 2002EUR
• 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	00841912100095 [Primary]
GS1	10841912100092 [Package]; Package: [10 Units]; Discontinued: 2020-02-14; Not in Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970889

FDA Product Code

• KKX: Drape, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2020-02-14
• Device Publish Date: 2016-09-16

On-Brand Devices [PullUp Surgical Probe Cover Kit]

• 10841912100849: 1938
• 00841912100262: 2005
• 00841912100101: 2002
• 00841912100095: 2002
• 00841912100088: 2002
• 10841912106414: 2002
• 10841912106278: 2002