FDA UDI In Commercial Distribution 🇺🇸 United States

PREVENTI

DI: 00850046528149 · Model: PRB2248 · Rushmedics LLC
Product Codes
3
GMDN Terms
1
Identifiers
3
Pkg Device Count
100

Basic Information

Brand Name
PREVENTI
Primary DI
00850046528149
Version / Model
PRB2248
Catalog Number
PRB2248
Company Name
Rushmedics LLC
Labeler DUNS
013526370
Distribution Status
In Commercial Distribution
Device Count in Pkg
100
Record Status
Published
Publish Date
2023-01-12
Public Version
1
Public Version Date
2023-01-20
Public Version Status
New
Public Device Record Key
17aa64e6-a119-489a-8d4f-3590216e2e2c

Device Description

PREVENTI- BIODEGRADABLE POWDER-FREE NITRILE EXAM GLOVES-X-LARGE

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 10850046528146
Primary 00850046528149
Unit of Use 20850046528143

Customer Contacts

Phone
+12252772255

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
41 – 104 Degrees Fahrenheit