CAPIJECT SAFETY LANCET

GUDID 80812608030275

Box of 200 Sterile Single-Use Lancing Device Blade 1.0

ASAHI POLYSLIDER COMPANY,LIMITED

Manual blood lancing device, single-use

• Primary Device ID: 80812608030275
• NIH Device Record Key: bf05eb4b-4e92-4bea-8aee-34745693a62f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAPIJECT SAFETY LANCET
• Version Model Number: 200101
• Company DUNS: 718296825
• Company Name: ASAHI POLYSLIDER COMPANY,LIMITED
• Device Count: 200
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	30389701009194 [Primary]
GS1	50389701009198 [Package]; Contains: 30389701009194; Package: Cardboard box [10 Units]; In Commercial Distribution
GS1	80812608030275 [Unit of Use]

FDA Product Code

• FMK: Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-08-09
• Device Publish Date: 2023-08-01

On-Brand Devices [CAPIJECT SAFETY LANCET]

• 50389701009235: Box of 200 Sterile Single-Use Lancing Device Needle 28G
• 50389701009228: Box of 200 Sterile Single-Use Lancing Device Needle 23G
• 50389701009211: Box of 200 Sterile Single-Use Lancing Device Blade 2.0
• 50389701009204: Box of 200 Sterile Single-Use Lancing Device Blade 1.5
• 80812608030275: Box of 200 Sterile Single-Use Lancing Device Blade 1.0