GOIO

GUDID 27290008325107

Intraosseous start kit by PerSys Medical

WaisMed Ltd

Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock Intravenous line stopcock 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