FDA UDI In Commercial Distribution 🇺🇸 United States

Liquinox

DI: 00660483120819 · Model: 8oz · ALCONOX INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Liquinox
Primary DI
00660483120819
Version / Model
8oz
Catalog Number
1208-1
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
9cc66abe-5bdf-4a20-944b-ef3e1417810d

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 00660483120819

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
15 – 30 Degrees Celsius