GOIO

GUDID 27290008325107

Intraosseous start kit by PerSys Medical

WaisMed Ltd

Intravenous line stopcock

• Primary Device ID: 27290008325107
• NIH Device Record Key: 9fc83012-9b30-42a8-8d59-87cb7c59cb2d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GOIO
• Version Model Number: GOIO without Fixation
• Company DUNS: 514619238
• Company Name: WaisMed Ltd
• 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: true
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	17290008325100 [Primary]
GS1	27290008325107 [Package]; Contains: 17290008325100; Package: [12 Units]; In Commercial Distribution

FDA Product Code

• GAX: Tourniquet, Nonpneumatic

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: 2021-04-14
• Device Publish Date: 2021-04-06

On-Brand Devices [GOIO]

• 27290008325015: Intraosseous start kit by PerSys Medical
• 27290008325107: Intraosseous start kit by PerSys Medical