Reti-TIC

GUDID 04061609000248

BIOANALYTIC GmbH, biomed. Analysentechnik

Reticulocyte count IVD, reagent

• Primary Device ID: 04061609000248
• NIH Device Record Key: ee516351-f277-4811-b0ee-2a704d5ce131
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reti-TIC
• Version Model Number: 004016-0006
• Company DUNS: 327536728
• Company Name: BIOANALYTIC GmbH, biomed. Analysentechnik
• 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: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04061609000248 [Primary]
GS1	04061609000613 [Unit of Use]

FDA Product Code

• JCG: Fluid, Diluting, Manual Cell

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2018-02-13

On-Brand Devices [Reti-TIC]

• 04061609000262: 004016-6010
• 04061609000248: 004016-0006