Ohio®

GUDID 06970966663103

0321-7825-800 is the suction jar which is used to collect pus, blood clots, phlegm, and excess fluids by connecting to a patient on one end, and vacuum source (such as suction regulator) on the other

GENTEC(SHANGHAI)CORPORATION

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• Primary Device ID: 06970966663103
• NIH Device Record Key: 2612bc1e-8518-41bb-ab96-cd740653f56d
• Commercial Distribution Discontinuation: 2031-11-09
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ohio®
• Version Model Number: 0321-7825-800
• Company DUNS: 545287658
• Company Name: GENTEC(SHANGHAI)CORPORATION
• Device Count: 1
• DM Exempt: true
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	06970966663103 [Primary]

FDA Product Code

• KDQ: Bottle, Collection, Vacuum

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: 2021-11-17
• Device Publish Date: 2021-11-09

On-Brand Devices [Ohio®]

• 06970966663103: 0321-7825-800 is the suction jar which is used to collect pus, blood clots, phlegm, and excess f
• 06970966663097: 0321-7815-800 is the suction jar which is used to collect pus, blood clots, phlegm, and excess f