O-RING PACK 002 O-RING KIT

GUDID D785002ORKIT0

002 O-Ring Kit

OCO BIOMEDICAL INC

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• Primary Device ID: D785002ORKIT0
• NIH Device Record Key: 5d55ec6a-a9bf-42a9-b7f8-008595ac6193
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: O-RING PACK
• Version Model Number: 002 O-Ring Kit
• Catalog Number: 002 O-RING KIT
• Company DUNS: 094146123
• Company Name: OCO BIOMEDICAL INC
• 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	D785002ORKIT0 [Primary]

FDA Product Code

• NDP: Accessories, Implant, Dental, Endosseous

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: 2024-04-11
• Device Publish Date: 2024-04-03

On-Brand Devices [O-RING PACK]

• D785003ORKIT0: 003 O-Ring Kit
• D785002ORKIT0: 002 O-Ring Kit