Mini Med 1001

GUDID B580IWX0

x-ray film processor, Medical

AFP MANUFACTURING, INC.

Dental automated x-ray film processor

• Primary Device ID: B580IWX0
• NIH Device Record Key: 8187a0b5-c150-49d3-9180-163aaba53713
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mini Med
• Version Model Number: Mini Med 90
• Catalog Number: 1001
• Company DUNS: 080326963
• Company Name: AFP MANUFACTURING, 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• 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
HIBCC	B580IWX0 [Primary]

FDA Product Code

• IXW: Processor, Radiographic-Film, Automatic

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: 2019-06-27
• Device Publish Date: 2019-06-19

Devices Manufactured by AFP MANUFACTURING, INC.

• B580EGY0 - AFP 810: 2019-06-27 x-ray film processor, dental
• B580IWX0 - Mini Med: 2019-06-27x-ray film processor, Medical
• B580IWX0 - Mini Med: 2019-06-27 x-ray film processor, Medical