FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERIFY

DI: 00724995002541 · Model: LCB030 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
VERIFY
Primary DI
00724995002541
Version / Model
LCB030
Catalog Number
LCB030
Company Name
STERIS CORPORATION
Labeler DUNS
868205779
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-01
Public Version
5
Public Version Date
2022-04-25
Public Version Status
Update
Public Device Record Key
4e01c04d-bee9-4370-87ab-4caabd335f34
Distribution End Date
2022-04-25

Device Description

The VERIFY Incubator is for exclusive use with VERIFY Assert Self-Contained Biological Indicators and VERIFY Process Challenge Devices.

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OWP Biological sterilization process indicator with recombinant-dna plasmid

GMDN Terms

Code Name
46944 Test tube heater

Identifiers

Type ID
Previous 00724995153052
Primary 00724995002541

Customer Contacts