FDA UDI In Commercial Distribution 🇺🇸 United States

Propper OK Sterilization Bags

DI: 70818087010022 · Model: 02101100 · PROPPER MANUFACTURING COMPANY, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1000

Basic Information

Brand Name
Propper OK Sterilization Bags
Primary DI
70818087010022
Version / Model
02101100
Company Name
PROPPER MANUFACTURING COMPANY, INC.
Labeler DUNS
001483130
Distribution Status
In Commercial Distribution
Device Count in Pkg
1000
Record Status
Published
Publish Date
2018-09-25
Public Version
2
Public Version Date
2021-02-19
Public Version Status
Update
Public Device Record Key
fe330c09-6699-45ca-a15e-bca1a11477b6

Device Description

Propper OK Sterilization Bags - 5.375" x 1.5" x 12" - 1 Case of 1000

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
Yes
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 70818087010022
Unit of Use 10818087010020