ADVOCATE Lancing Device Lianfa LD Lianfa

GUDID 00894046001974

Advocate Lancing Device Lianfa, adjustable device allowing selection of appropriate depth penetration for maximum comfort in acquiring a capillary blood sample to monitor blood glucose levels

DIABETIC SUPPLY OF SUNCOAST, INC.

Manual blood lancing device, single-use

• Primary Device ID: 00894046001974
• NIH Device Record Key: 81a57670-9422-4816-9b6d-ffeb8c524769
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ADVOCATE Lancing Device Lianfa
• Version Model Number: 328-B
• Catalog Number: LD Lianfa
• Company DUNS: 043081723
• Company Name: DIABETIC SUPPLY OF SUNCOAST, 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: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: 18884693579
• Email: lhenry@pharmasupply.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00894046001974 [Primary]

FDA Product Code

• FMK: Lancet, Blood

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: 2020-06-30
• Device Publish Date: 2020-06-22

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