1806-0085S

GUDID 04546540195937

Guide Wire, Ball-Tipped, sterile

Stryker Trauma GmbH

Bone nail guidewire, reusable

• Primary Device ID: 04546540195937
• NIH Device Record Key: 77ed67bb-7e55-4a45-bd47-4e94190d655b
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 1806-0085S
• Catalog Number: 1806-0085S
• Company DUNS: 330211587
• Company Name: Stryker Trauma GmbH
• 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: true
• 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

• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter
• Device Size Text, specify: 0
• Length: 1000 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540195937 [Primary]

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: 2020-04-15
• Device Publish Date: 2020-04-07

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