TruePoint 64233

GUDID 00193169642331

Blood Glucose Test Strips

OK BIOTECH CO., LTD.

Glucose IVD, kit, electrometry

• Primary Device ID: 00193169642331
• NIH Device Record Key: 64e88865-8c9b-42f0-8062-37a55db6251a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TruePoint
• Version Model Number: 64233
• Catalog Number: 64233
• Company DUNS: 658796458
• Company Name: OK BIOTECH CO., LTD.
• Device Count: 150
• DM Exempt: false
• 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: true
• Lot Batch: false
• 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	00193169642331 [Primary]
GS1	50193169642305 [Unit of Use]

FDA Product Code

• NBW: System, Test, Blood Glucose, Over The Counter

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: 2019-01-03
• Device Publish Date: 2018-12-03

On-Brand Devices [TruePoint]

• 00193169642409: Blood Glucose Test Strips
• 00193169642362: Blood Glucose Test Strips
• 00193169642348: Blood Glucose Test Strips
• 00193169642331: Blood Glucose Test Strips
• 00193169642324: Blood Glucose Test Strips
• 10193169642307: Blood Glucose Test Strips