FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERIFY

DI: 50724995153217 · Model: LCB042 · STERIS CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
50

Basic Information

Brand Name
VERIFY
Primary DI
50724995153217
Version / Model
LCB042
Catalog Number
LCB042
Company Name
STERIS CORPORATION
Labeler DUNS
040469731
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
50
Record Status
Published
Publish Date
2019-04-19
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
b4d2e90c-a0a0-440e-b20b-65ed014d7e4a
Distribution End Date
2020-09-11

Device Description

The VERIFY All-In-One PV10 Assembly is a single-use plastic tube that is designed to hold a biological indicator in place during the steam sterilization process.

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
No
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
35362 Chemical/physical sterilization process indicator

Identifiers

Type ID
Primary 50724995153217
Unit of Use 00724995153212

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K103321 000
K173633 000
K182931 000