Ammonia II 08058024190

GUDID 07613336121429

Roche Diagnostics GmbH

Ammonia IVD, kit, enzyme spectrophotometry

• Primary Device ID: 07613336121429
• NIH Device Record Key: 0fb3a31c-245b-46f3-b449-5c17cd71714f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ammonia II
• Version Model Number: 08058024190
• Catalog Number: 08058024190
• Company DUNS: 315028860
• Company Name: Roche Diagnostics GmbH
• 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: 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: true
• OTC Over-The-Counter: false

Operating and Storage Conditions

• Storage Environment Temperature: Between 2 Degrees Celsius and 8 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613336121429 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183517

FDA Product Code

• JIF: ENZYMATIC METHOD, AMMONIA

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: 2020-03-13
• Device Publish Date: 2020-03-05

On-Brand Devices [Ammonia II]

• 04015630936526: 07229593190
• 04015630936533: 07236450190
• 07613336121429: 08058024190