FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERIFY

DI: 10724995021471 · Model: 810110 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
250

Basic Information

Brand Name
VERIFY
Primary DI
10724995021471
Version / Model
810110
Catalog Number
810110
Company Name
STERIS CORPORATION
Labeler DUNS
961394798
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
250
Record Status
Published
Publish Date
2016-09-09
Public Version
5
Public Version Date
2019-07-03
Public Version Status
Update
Public Device Record Key
66a15749-2ed8-4c31-b765-f96e9eb21dda
Distribution End Date
2019-06-21

Device Description

The VERIFY Dual Integrators monitor all critical parameters of steam (temperature, time and steam quality) and ethylene oxide sterilization (time, temperature, gas concentration and humidity).

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
FRC Indicator, biological sterilization process

GMDN Terms

Code Name
13732 Biological sterilization indicator

Identifiers

Type ID
Primary 10724995021471
Unit of Use 00724995021474

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K800029 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store away from sterilizers
Type
Special Storage Condition, Specify
Special Conditions
Avoid Sterilant or Cleaning Chemicals
Type
Special Storage Condition, Specify
Special Conditions
Store at room temperature.