FDA UDI In Commercial Distribution 🇺🇸 United States

ML 830®

DI: 00859626006077 · Model: ML-830-01-009 · MICROLIGHT CORPORATION OF AMERICA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ML 830®
Primary DI
00859626006077
Version / Model
ML-830-01-009
Catalog Number
ML-830-01-009
Company Name
MICROLIGHT CORPORATION OF AMERICA
Labeler DUNS
137829417
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-08-15
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
5b6d3f74-bc5c-4407-888c-f3f94e823a65

Device Description

Large Danger Sign

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
NHN Powered Light Based Non-Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy

GMDN Terms

Code Name
15928 Safety sign

Identifiers

Type ID
Primary 00859626006077

Customer Contacts

Phone
281-433-4648