Prodigy Pressure Activated Safety Lancets 24-082341

GUDID 30384840823410

Prodigy Pressure Activated Safety Lancets 21G (100 ct)

PRODIGY DIABETES CARE, LLC

Manual blood lancing device, single-use

• Primary Device ID: 30384840823410
• NIH Device Record Key: b5ffbbb3-ea1c-44c7-8187-5f324cefd430
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Prodigy Pressure Activated Safety Lancets
• Version Model Number: 24-082341
• Catalog Number: 24-082341
• Company DUNS: 832875905
• Company Name: PRODIGY DIABETES CARE, LLC
• Device Count: 100
• 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: 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: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00384840823419 [Primary]
GS1	30384840823410 [Package]; Contains: 00384840823419; Package: Corrugated Box [10 Units]; In Commercial Distribution
GS1	90384840823412 [Unit of Use]

FDA Product Code

• FMK: Lancet, Blood

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: 2018-09-21
• Device Publish Date: 2018-08-21

On-Brand Devices [Prodigy Pressure Activated Safety Lancets]

• 30384849903380: Prodigy Pressure Activated Safety Lancets 28G (100 ct)
• 30384840823410: Prodigy Pressure Activated Safety Lancets 21G (100 ct)
• 00384840823167: Prodigy Pressure Activated Safety Lancets 26G (100 ct)