LA Cartridge 070810

GUDID 00856522006071

LA Cartridge, 10 count

Lifehealth

Lactate IVD, reagent

• Primary Device ID: 00856522006071
• NIH Device Record Key: 63db8e40-4452-4f8b-908f-ca3cb2ae362b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: LA Cartridge
• Version Model Number: 078770
• Catalog Number: 070810
• Company DUNS: 080886029
• Company Name: Lifehealth
• Device Count: 10
• 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: 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

Customer Support Contacts

• Phone: 1-651-638-1000
• Email: cs@lifehealthmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00856522006071 [Primary]
GS1	00856522006163 [Unit of Use]

FDA Product Code

• KHP: Acid, Lactic, Enzymatic Method

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [LA Cartridge]

• 00856522006071: LA Cartridge, 10 count
• 00856522006040: LA Cartridge, 25 count