LimaCorporate Kirschner wire 9095.11.952.S

GUDID 08033390190176

Dia. 2,5 x 200 mm - K-wire Sterile

LIMACORPORATE SPA

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• Primary Device ID: 08033390190176
• NIH Device Record Key: 6d33b887-361f-4b63-a399-f889321accba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LimaCorporate Kirschner wire
• Version Model Number: 9095.11.952.S
• Catalog Number: 9095.11.952.S
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• 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: 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

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Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390190176 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203475

FDA Product Code

• HTY: Pin, Fixation, Smooth

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: 2021-03-26
• Device Publish Date: 2021-03-18

On-Brand Devices [LimaCorporate Kirschner wire]

• 08033390190183: Dia. 2,5 x 150 mm - K-wire Sterile
• 08033390190176: Dia. 2,5 x 200 mm - K-wire Sterile
• 08033390188494: Dia. 2,5 x 240 mm - K-wire Sterile