α-spot

GUDID 10850039198035

LFP Alpha-Spot Kit

EASTERN BUSINESS FORMS INC

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• Primary Device ID: 10850039198035
• NIH Device Record Key: db8118c7-1d4a-4a6c-88b8-c6c975fb7c81
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: α-spot
• Version Model Number: W221
• Company DUNS: 079861573
• Company Name: EASTERN BUSINESS FORMS 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: true
• Device Combination Product: false
• Single Use: true
• 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	00850039198038 [Primary]
GS1	10850039198035 [Package]; Contains: 00850039198038; Package: [50 Units]; In Commercial Distribution

FDA Product Code

• JKA: Tubes, Vials, Systems, Serum Separators, Blood Collection

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: 2024-01-19
• Device Publish Date: 2024-01-11

On-Brand Devices [α-spot]

• 00860802000390: LFP Alpha-Spot Kit
• 10850039198035: LFP Alpha-Spot Kit