FDA UDI In Commercial Distribution 🇺🇸 United States

VERIFY

DI: 10724995172234 · Model: RK019 · ALBERT BROWNE LIMITED
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
VERIFY
Primary DI
10724995172234
Version / Model
RK019
Catalog Number
RK019
Company Name
ALBERT BROWNE LIMITED
Labeler DUNS
218172765
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2020-05-29
Public Version
4
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
af7d0546-3710-4213-bb94-0336d21a11b6

Device Description

The VERIFY Steam and EO Load Record Cards document load contents and confirm the load has been processed.

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
JOJ Indicator, physical/chemical sterilization process

GMDN Terms

Code Name
35362 Chemical/physical sterilization process indicator

Identifiers

Type ID
Unit of Use 00724995172237
Primary 10724995172234
Previous 10724995096714

Customer Contacts