FDA UDI In Commercial Distribution 🇺🇸 United States

Propper

DI: 70818087011777 · Model: Once-A-Day Bowie Dick Test · PROPPER MANUFACTURING COMPANY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Basic Information

Brand Name
Propper
Primary DI
70818087011777
Version / Model
Once-A-Day Bowie Dick Test
Catalog Number
26610300
Company Name
PROPPER MANUFACTURING COMPANY, INC.
Labeler DUNS
001483130
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2016-09-09
Public Version
4
Public Version Date
2021-12-27
Public Version Status
Update
Public Device Record Key
842cc2f1-369e-4805-9ec9-59812e66cf09

Device Description

INDICATOR STEAM OAD BOWIE DICK

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Primary 70818087011777
Unit of Use 10818087011775

Premarket Submissions

Submission Number Supplement Number
K961156 000