FDA UDI In Commercial Distribution 🇺🇸 United States

VERIFY

DI: 00724995218539 · Model: Bowie Dick · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
VERIFY
Primary DI
00724995218539
Version / Model
Bowie Dick
Catalog Number
EQC009
Company Name
STERIS CORPORATION
Labeler DUNS
868205779
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-11-07
Public Version
1
Public Version Date
2022-11-15
Public Version Status
New
Public Device Record Key
8c503bf3-0090-4896-84c9-094761a36eec

Device Description

The VERIFY Bowie Dick Test Pack Air Removal is designed to monitor air removal and steam penetration during the preconditioning phase of some pre-vacuum steam sterilizer processing cycles.

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
Package 10724995218536
Primary 00724995218539
Previous 10724995084568

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K002741 000
K162758 000

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
30 – 60 Percent (%) Relative Humidity
Type
Special Storage Condition, Specify
Special Conditions
Avoid Direct Light
Type
Storage Environment Temperature
Temperature Range
32 – 86 Degrees Fahrenheit