FDA UDI In Commercial Distribution 🇺🇸 United States

VERIFY

DI: 10724995024007 · Model: S3095 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
31

Basic Information

Brand Name
VERIFY
Primary DI
10724995024007
Version / Model
S3095
Catalog Number
S3095
Company Name
STERIS CORPORATION
Labeler DUNS
961394798
Distribution Status
In Commercial Distribution
Device Count in Pkg
31
Record Status
Published
Publish Date
2016-09-09
Public Version
6
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
47d6b13b-380c-4db6-b8d9-b2c4ff29ffc6

Device Description

The VERIFY Bowie Dick Test Card is a pre-assembled Bowie-Dick test pack product. The Card is the test and offers a convenient system for testing prevacuum sterilizers.

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 10724995024007
Unit of Use 00724995024000

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Relative Humidity not to exceed 70% before and after processing
Type
Storage Environment Temperature
Temperature Range
59 – 86 Degrees Fahrenheit