Ammonia

Basic Information

• Brand Name: Ammonia
• Primary DI: 04015630927005
• Version / Model: 05401739190
• Catalog Number: 05401739190
• Company Name: Roche Diagnostics GmbH
• Labeler DUNS: 315028860
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2021-02-08
• Public Version: 3
• Public Version Date: 2021-08-13
• Public Version Status: Update
• Public Device Record Key: 4dbef540-cb82-4fee-ad1d-ca341d559fca

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: No
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
JIF	ENZYMATIC METHOD, AMMONIA	Clinical Chemistry	862.1065	1

GMDN Terms

Code	Name	Definition	Implantable	Status
53203	Ammonia IVD, kit, enzyme spectrophotometry	A collection of reagents and other associated materials intended to be used for the qualitative and/or quantitative detection of ammonia in a clinical specimen, using an enzyme spectrophotometry method.	No	Obsolete

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	04015630927005	GS1

Premarket Submissions

Submission Number	Supplement Number
K972250	000