UREA NITROGEN (BERTHELOT) 2290-L

GUDID 00852223007119

UREA NITROGEN/COLOR (BERTHELOT)

STERLING DIAGNOSTICS INC

Urea IVD, reagent

• Primary Device ID: 00852223007119
• NIH Device Record Key: f5ee06d6-03e1-4825-9b85-a4be733a8e18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: UREA NITROGEN (BERTHELOT)
• Version Model Number: 2290-L
• Catalog Number: 2290-L
• Company DUNS: 155284151
• Company Name: STERLING DIAGNOSTICS INC
• 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: true
• Device Combination Product: false
• Single Use: false
• 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	00852223007119 [Primary]

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: 2018-04-17
• Device Publish Date: 2016-09-14

On-Brand Devices [UREA NITROGEN (BERTHELOT)]

• 00852223007126: UREA NITROGEN (BERTHELOT)
• 00852223007119: UREA NITROGEN/COLOR (BERTHELOT)