FDA UDI In Commercial Distribution 🇺🇸 United States

Revital-Ox

DI: 00724995216900 · Model: 4454AW · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Revital-Ox
Primary DI
00724995216900
Version / Model
4454AW
Catalog Number
4454AW
Company Name
STERIS CORPORATION
Labeler DUNS
139424188
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-17
Public Version
1
Public Version Date
2024-04-25
Public Version Status
New
Public Device Record Key
228dad3b-a85b-43f0-9627-9259052aad71

Device Description

Revital-Ox PAA HLD Solution Part B is used Revital-Ox PAA HLD Part A and the enspire 300 Series Automated Endoscope Reprocessor

Device Characteristics

Single Use
Yes
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
No
Has Manufacturing Date
Yes
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 50724995216905
Primary 00724995216900

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K230560 000
K232918 000