FDA UDI In Commercial Distribution 🇺🇸 United States

UltrOx

DI: 10841436123157 · Model: 610-2473 · CIVCO MEDICAL INSTRUMENTS CO., INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
UltrOx
Primary DI
10841436123157
Version / Model
610-2473
Catalog Number
610-2473
Company Name
CIVCO MEDICAL INSTRUMENTS CO., INC.
Labeler DUNS
134614411
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-03
Public Version
1
Public Version Date
2023-05-11
Public Version Status
New
Public Device Record Key
d8ca87a1-32a5-4a6e-b6f9-39a5752cc4c8

Device Description

UltrOx High Level Disinfectant

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
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
MED Sterilant, medical devices

GMDN Terms

Code Name
47631 Medical device disinfection agent

Identifiers

Type ID
Package 00841436123150
Primary 10841436123157

Customer Contacts