VEVOR

Basic Information

• Brand Name: VEVOR
• Primary DI: 06950940802124
• Version / Model: AST-300L
• Company Name: Shenzhen Osto Technology Co.,Ltd.
• Labeler DUNS: 528161684
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 201
• Record Status: Published
• Publish Date: 2024-08-20
• Public Version: 1
• Public Version Date: 2024-08-28
• Public Version Status: New
• Public Device Record Key: 95649966-71b0-4480-80c6-1e37d81058a6

Device Characteristics

• Single Use: No
• Prescription Use (Rx): No
• 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: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: No
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
NGX	Stimulator, Muscle, Powered, For Muscle Conditioning	Physical Medicine	890.5850	2
NUH	Stimulator, Nerve, Transcutaneous, Over-The-Counter	Neurology	882.5890	2

GMDN Terms

Code	Name	Definition	Implantable	Status
52816	Respiratory syncytial virus (RSV) immunoglobulin G (IgG)/IgM antibody IVD, control	A material which is used to verify the performance of an assay intended to be used for the qualitative and/or quantitative detection of immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies to respiratory syncytial virus (RSV) in a clinical specimen.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Unit of Use	06950940802131	GS1
Primary	06950940802124	GS1

Premarket Submissions

Submission Number	Supplement Number
K190783	000