Validate

Basic Information

• Brand Name: Validate
• Primary DI: 00859110005142
• Version / Model: 904se
• Catalog Number: 904se
• Company Name: Lgc Clinical Diagnostics, Inc.
• Labeler DUNS: 075886031
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2018-01-18
• Public Version: 3
• Public Version Date: 2022-02-24
• Public Version Status: Update
• Public Device Record Key: eaa81f3b-7bf2-4e26-a77c-feeb406b1c51

Device Description

Validate Fibrinogen is intended for the quantitative determination of Calibration Verification/Linearity of fibrinogen on automated instruments.

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: Yes
• 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: Yes
• 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
GIL	Plasma, Fibrinogen Control	Hematology	864.7340	2

GMDN Terms

Code	Name	Definition	Implantable	Status
32393	Fibrinogen assay (factor I) IVD, control	A material which is used to verify the performance of an assay intended to be used for the quantitative measurement of fibrinogen (factor I) in a clinical specimen.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00859110005142	GS1

Customer Contacts

• Phone: [phone]
• Email: [email protected]

Device Sizes

Type	Value	Unit	Text
Device Size Text, specify			1 test

Storage Conditions

• Type: Storage Environment Temperature
• Temperature Range: -25 – -10 Degrees Celsius