Director Biopsy/Needle Guide/Probe Cover Kit 4222

GUDID 10841912101136

PROTEK MEDICAL PRODUCTS, INC.

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• Primary Device ID: 10841912101136
• NIH Device Record Key: c8741e41-d98c-4c4a-96fa-c4a5f2530de0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Director Biopsy/Needle Guide/Probe Cover Kit
• Version Model Number: 4222
• Catalog Number: 4222
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841912101139 [Primary]
GS1	10841912101136 [Package]; Contains: 00841912101139; Package: [24 Units]; In Commercial Distribution
GS1	20841912101133 [Package]; Contains: 00841912101139; Package: [12 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K970893

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: 6
• Public Version Date: 2019-10-07
• Device Publish Date: 2016-09-16

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• 10841912105479: 4221
• 00841912104468: 4222
• 00841912104451: 4220
• 00841912104444: 4218
• 00841912104437: 4216
• 10841912101136: 4222
• 10841912101129: 4220
• 10841912101112: 4218
• 00841912101108: 4216