Turbett Surgical

GUDID 00859464007281

Turbett Surgical TS1200 Container

Turbett Surgical Inc

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• Primary Device ID: 00859464007281
• NIH Device Record Key: c646a0f7-a61d-4b5c-aff9-411de5952d20
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Turbett Surgical
• Version Model Number: TS1200
• Company DUNS: 080273036
• Company Name: Turbett Surgical Inc
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00859464007281 [Primary]

FDA Product Code

• FRG: Wrap, Sterilization

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-18
• Device Publish Date: 2023-07-10

On-Brand Devices [Turbett Surgical]

• 00859464007281: Turbett Surgical TS1200 Container
• 00859464007212: Turbett Surgical TS1000 containers
• 00859464007113: TS1500 Container