LITe FC-140-22-B-4

GUDID 37613327343565

Y-Wire (pack of 4)

Stryker Corporation

Spinal guidewire

• Primary Device ID: 37613327343565
• NIH Device Record Key: b9016ede-d0cc-4bdb-96a5-93f9f53b1ae6
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LITe
• Version Model Number: FC-140-22-B-4
• Catalog Number: FC-140-22-B-4
• Company DUNS: 149183167
• Company Name: Stryker Corporation
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0
• Length: 559 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327343564 [Primary]
GS1	37613327343565 [Package]; Contains: 07613327343564; Package: pack [5 Units]; In Commercial Distribution

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-12-23
• Device Publish Date: 2019-12-13

On-Brand Devices [LITe]

• 07613327359619: Y-Needle 200
• 07613327359602: Funnel
• 07613327359596: Y-Needle 400
• 07613327359589: Y-Needle 300
• 07613327359572: Y-Needle 100
• 37613327343565: Y-Wire (pack of 4)
• 37613327343558: Y-Wire (pack of 4)
• 37613327343541: Y-Wire (pack of 2)
• 37613327343534: Y-Wire (pack of 2)
• 37613327343527: Y-Wire (pack of 2)
• 37613327343510: Y-Wire (pack of 4)
• 37613327343480: Y-Wire (pack of 4) ES2 Compatible
• 37613327343459: Y-Wire (pack of 4)
• 37613327343442: Y-Wire (pack of 2)
• 37613327343435: Y-Wire (pack of 2) ES2 Compatible