FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERIFY

DI: 10724995085671 · Model: LCB007 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
20

Basic Information

Brand Name
VERIFY
Primary DI
10724995085671
Version / Model
LCB007
Catalog Number
LCB007
Company Name
STERIS CORPORATION
Labeler DUNS
961394798
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
20
Record Status
Published
Publish Date
2016-09-09
Public Version
6
Public Version Date
2023-04-21
Public Version Status
Update
Public Device Record Key
b33cb485-715c-4a08-bb94-a0153cca0f12
Distribution End Date
2023-04-20

Device Description

The VERIFY Biological Integrator Challenge Packs are used to release dynamic air removal (prevacuum and steam-flush pressure-pulse) and steam sterilization (autoclave) 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
FRC Indicator, biological sterilization process

GMDN Terms

Code Name
13732 Biological sterilization indicator

Identifiers

Type ID
Primary 10724995085671
Unit of Use 00724995085674

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from direct light
Type
Special Storage Condition, Specify
Special Conditions
Do not Freeze
Type
Storage Environment Temperature
Temperature Range
59 – 77 Degrees Fahrenheit
Type
Storage Environment Humidity
Temperature Range
35 – 60 Percent (%) Relative Humidity