Autolet

GUDID 00384700270025

Autolet Lancing Device

OWEN MUMFORD USA INCORPORATED

Manual blood lancing device, reusable

• Primary Device ID: 00384700270025
• NIH Device Record Key: 980e158f-da07-4d14-98f8-13f002fa4120
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Autolet
• Version Model Number: At 0270
• Company DUNS: 803401454
• Company Name: OWEN MUMFORD USA INCORPORATED
• Device Count: 1
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00384700270018 [Primary]
GS1	00384700270025 [Package]; Contains: 00384700270018; Package: Sleeve [20 Units]; In Commercial Distribution
GS1	00384700270032 [Package]; Package: Case [10 Units]; In Commercial Distribution

FDA Product Code

• QRL: Multiple Use Blood Lancet For Single Patient Use Only

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: 2023-02-15
• Device Publish Date: 2023-02-07

On-Brand Devices [Autolet]

• 00384700270025: Autolet Lancing Device
• 00384700271039: Autolet Lancing Device
• 00384700272012: Autolet Lancing Device with 10 30G lancets in a bag