FDA UDI In Commercial Distribution 🇺🇸 United States

Plasti-Products

DI: 10797876143012 · Model: 143020 · PLASTI-PRODUCTS INC
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
Plasti-Products
Primary DI
10797876143012
Version / Model
143020
Company Name
PLASTI-PRODUCTS INC
Labeler DUNS
153880372
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-20
Public Version
4
Public Version Date
2023-08-18
Public Version Status
Update
Public Device Record Key
803289bb-b727-419f-ba6d-a56bb04cdf9c

Device Description

sharps container, yellow, 5qt

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
FMI Needle, Hypodermic, Single Lumen

GMDN Terms

Code Name
35429 Sharps container

Identifiers

Type ID
Package 40797876143013
Package 20797876143019
Primary 10797876143012

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K970383 000