Dilution Plate, Phadia 250

Basic Information

• Brand Name: Dilution Plate, Phadia 250
• Primary DI: 07333066001036
• Version / Model: 12-3907-08
• Catalog Number: 12-3907-08
• Company Name: Phadia AB
• Labeler DUNS: 354019424
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2019-02-20
• Public Version: 3
• Public Version Date: 2023-12-11
• Public Version Status: Update
• Public Device Record Key: 6545fb71-cc8a-4564-b054-fe7f2aa41513

Device Description

Dilution Plate, Phadia 250

Device Characteristics

• Single Use: No
• 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: Yes
• Has Expiration Date: No
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NHX	ANTIBODIES, ANTI-CYCLIC CITRULLINATED PEPTIDE (CCP)	Immunology	866.5775	2

GMDN Terms

Code	Name	Definition	Implantable	Status
53961	Plasma protein IVD, reagent	A substance or reactant intended to be used together with a parent IVD to perform a specific function in an assay that is used for the quantitative measurement of plasma proteins in a clinical specimen.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	07333066001036	GS1

Customer Contacts

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