MD DrugScreen

Basic Information

• Brand Name: MD DrugScreen
• Primary DI: 00860007913167
• Version / Model: MDC-6135F
• Company Name: Medical Disposables Corp
• Labeler DUNS: 961673774
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2026-03-18
• Public Version: 1
• Public Version Date: 2026-03-26
• Public Version Status: New
• Public Device Record Key: 541cc36d-0aa9-41f9-8908-8c91d3e7f7fd

Device Description

MDC-6135F CLIA WAIVED 13 Panel Cup w/Fen (AMP1000/BAR300/BUP10/BZO300/COC300/FEN300/MDMA500/ OPI300/MTD300/MET1000/OXY100/PCP25/THC50)

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): No
• Over the Counter (OTC): Yes
• Kit: Yes
• Combination Product: No
• HCT/P: No
• Contains NRL: Yes
• 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
QDO	Fentanyl And Other Opioid Protection Glove	General Hospital	880.6250	1

GMDN Terms

Code	Name	Definition	Implantable	Status
46994	Multiple drugs of abuse IVD, kit, rapid ICT, clinical	A collection of reagents and other associated materials intended to be used for the qualitative and/or (semi-)quantitative detection of multiple drugs of abuse in a clinical specimen within a short period, relative to standard laboratory testing procedures, using an immunochromatographic test (ICT) method [lateral flow test]. This is a rapid test used in the laboratory or in point-of-care analyses. It is not intended to be used for self-testing.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00860007913167	GS1