FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERIFY

DI: 00724995153052 · Model: LCB030 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VERIFY
Primary DI
00724995153052
Version / Model
LCB030
Catalog Number
LCB030
Company Name
STERIS CORPORATION
Labeler DUNS
961394798
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-27
Public Version
5
Public Version Date
2019-04-01
Public Version Status
Update
Public Device Record Key
6ebbcf3a-3790-40b3-81e9-d4e66815d22f
Distribution End Date
2019-04-01

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
Primary 00724995153052

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K163587 000