FDA UDI In Commercial Distribution 🇺🇸 United States

PREVENTI

DI: 00850046528064 · Model: PRN1921 · Rushmedics LLC
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
250

Basic Information

Brand Name
PREVENTI
Primary DI
00850046528064
Version / Model
PRN1921
Catalog Number
PRN1921
Company Name
Rushmedics LLC
Labeler DUNS
013526370
Distribution Status
In Commercial Distribution
Device Count in Pkg
250
Record Status
Published
Publish Date
2022-11-12
Public Version
2
Public Version Date
2022-12-22
Public Version Status
Update
Public Device Record Key
f1c29945-16e3-4761-aed9-07de583bdba1

Device Description

PREVENTI-LOW-DERMATITIS POWDER-FREE NITRILE EXAM GLOVES-SMALL

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
Yes
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LZA Polymer Patient Examination Glove
LZC Patient Examination Glove, Specialty
QDO Fentanyl And Other Opioid Protection Glove

GMDN Terms

Code Name
56286 Nitrile examination/treatment glove, non-powdered, non-antimicrobial

Identifiers

Type ID
Package 10850046528061
Primary 00850046528064
Unit of Use 20850046528068

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
41 – 104 Degrees Fahrenheit