FDA UDI Not in Commercial Distribution 🇺🇸 United States

SteriScan

DI: 10724995152281 · Model: 5500 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
100

Basic Information

Brand Name
SteriScan
Primary DI
10724995152281
Version / Model
5500
Catalog Number
5500
Company Name
STERIS CORPORATION
Labeler DUNS
040469731
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2016-09-13
Public Version
7
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
3af5d566-bf3e-4e20-84f3-5ff21a0310f4
Distribution End Date
2020-09-11

Device Description

The SteriScan Bowie Dick Indicator is for exclusive use with the VERIFY All-In-One STEAM Reusable Test Pack.

Device Characteristics

Single Use
Yes
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
JOJ Indicator, physical/chemical sterilization process

GMDN Terms

Code Name
35362 Chemical/physical sterilization process indicator

Identifiers

Type ID
Primary 10724995152281
Unit of Use 00724995152284

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120592 000