FDA UDI In Commercial Distribution 🇺🇸 United States

VERIFY

DI: 10724995180291 · Model: LCB005 · STERIS CORPORATION
Product Codes
2
GMDN Terms
1
Identifiers
3
Pkg Device Count
5

Basic Information

Brand Name
VERIFY
Primary DI
10724995180291
Version / Model
LCB005
Catalog Number
LCB005
Company Name
STERIS CORPORATION
Labeler DUNS
961394798
Distribution Status
In Commercial Distribution
Device Count in Pkg
5
Record Status
Published
Publish Date
2021-04-20
Public Version
2
Public Version Date
2022-10-17
Public Version Status
Update
Public Device Record Key
6c82c86f-ecaa-40d7-96a6-a09b2306e0a0

Device Description

The VERIFY V24 Challenge Pack is for qualifications testing of the V-PRO Low Temperature Sterilization Systems following installation, relocation, malfunctions or major repairs.

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
No
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
JOJ Indicator, physical/chemical sterilization process

GMDN Terms

Code Name
13732 Biological sterilization indicator

Identifiers

Type ID
Unit of Use 00724995180294
Previous 10724995084674
Primary 10724995180291

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
40 – 60 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
70 – 77 Degrees Fahrenheit
Type
Special Storage Condition, Specify
Special Conditions
Keep away from direct light