DRYPRO MODEL 873

GUDID 04560141923126

KONICA MINOLTA, INC.

Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera Diagnostic-imaging multiformat camera

• Primary Device ID: 04560141923126
• NIH Device Record Key: 35f1024e-6252-406c-9ffa-61da6b5fcf38
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DRYPRO MODEL 873
• Version Model Number: A2MM
• Company DUNS: 692076161
• Company Name: KONICA MINOLTA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• 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	04560141923126 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081637

FDA Product Code

• LMC: Camera, Multi Format, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-10-29
• Device Publish Date: 2016-09-19

On-Brand Devices [DRYPRO MODEL 873]

• 04560141923126: A2MM
• 04560141923119: A2GP
• 04560141950474: AE1T