N/M

GUDID 06949517006201

Shandong Lianfa Medical Plastic Products CO.,LTD

Manual blood lancing device, reusable

• Primary Device ID: 06949517006201
• NIH Device Record Key: b8ea2b0d-a3c7-4a70-8989-69a674eb53d9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: N/M
• Version Model Number: LDC
• Company DUNS: 421330121
• Company Name: Shandong Lianfa Medical Plastic Products CO.,LTD
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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	06949517006201 [Primary]

FDA Product Code

• QRK: Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

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: 2026-02-09
• Device Publish Date: 2026-01-31

On-Brand Devices [N/M]

• 06949517007024: Lancing Device(Bag of 1 devices)
• 06949517009462: LDC
• 06949517006201: LDC