Sterile Disposable Endocavity Needle Guide 5178

GUDID 10841912101709

PROTEK MEDICAL PRODUCTS, INC.

Body-orifice ultrasound imaging transducer cover, basic, sterile

• Primary Device ID: 10841912101709
• NIH Device Record Key: 8873997f-8e70-49e7-951d-3663edc08d77
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Sterile Disposable Endocavity Needle Guide
• Version Model Number: 5178
• Catalog Number: 5178
• 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: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841912101702 [Primary]
GS1	10841912101709 [Package]; Contains: 00841912101702; Package: [24 Units]; In Commercial Distribution

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

On-Brand Devices [Sterile Disposable Endocavity Needle Guide]

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• 10841912104878: 5370
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• 10841912103857: 5142
• 10841912101839: 9003
• 10841912101822: 9002
• 10841912101815: 9001
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• 10841912101761: 5531
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• 10841912101716: 5380
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• 10841912101624: 5145
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• 10841912101587: 5070
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• 10841912106124: 5281
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