FDA UDI In Commercial Distribution 🇺🇸 United States

Luminox

DI: 00660483190140 · Model: 4x1 case · ALCONOX INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Luminox
Primary DI
00660483190140
Version / Model
4x1 case
Catalog Number
1901
Company Name
ALCONOX INC
Labeler DUNS
001478726
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-02
Public Version
1
Public Version Date
2020-10-12
Public Version Status
New
Public Device Record Key
e3d110ca-816a-4b6f-be39-175b7c8a6891

Device Description

Cleaner for ultrasonic cleaning of medical devices

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
Yes
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
FLG Cleaner, Ultrasonic, Medical Instrument

GMDN Terms

Code Name
63385 Medical device cleaning agent

Identifiers

Type ID
Primary 00660483190140