PREVENTI PRN1922

GUDID 10850046528078

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

Rushmedics LLC

Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial Nitrile examination/treatment glove, non-powdered, non-antimicrobial
Primary Device ID10850046528078
NIH Device Record Key0c305d10-290f-47f1-9f2f-51e51457e204
Commercial Distribution StatusIn Commercial Distribution
Brand NamePREVENTI
Version Model NumberPRN1922
Catalog NumberPRN1922
Company DUNS013526370
Company NameRushmedics LLC
Device Count250
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com
Phone+1 (225) 277-2255
Emailcontact@rushmedics.com

Operating and Storage Conditions

Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit
Handling Environment TemperatureBetween 41 Degrees Fahrenheit and 104 Degrees Fahrenheit

Device Identifiers

Device Issuing AgencyDevice ID
GS100850046528071 [Primary]
GS110850046528078 [Package]
Contains: 00850046528071
Package: CASE [10 Units]
In Commercial Distribution
GS120850046528075 [Unit of Use]

FDA Product Code

LZAPolymer Patient Examination Glove

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-11-21
Device Publish Date2022-11-12

On-Brand Devices [PREVENTI]

10850046528092PREVENTI- LOW-DERMATITIS POWDER-FREE NITRILE EXAM GLOVES- X-LARGE
10850046528085PREVENTI- LOW-DERMATITIS POWDER-FREE NITRILE EXAM GLOVES- LARGE
10850046528078PREVENTI- LOW-DERMATITIS POWDER-FREE NITRILE EXAM GLOVES-MEDIUM
10850046528061PREVENTI-LOW-DERMATITIS POWDER-FREE NITRILE EXAM GLOVES-SMALL
10850046528054PREVENTI- LOW-DERMATITIS POWDER-FREE NITRILE EXAM GLOVES-X-SMALL
10850046528047PREVENTI- BIODEGRADABLE POWDER-FREE NITRILE EXAM GLOVES- X-LARGE
10850046528030PREVENTI- POWDER- BIODEGRADABLE FREE NITRILE EXAM GLOVES-LARGE
10850046528023PREVENTI-BIODEGRADABLE POWDER-FREE NITRILE EXAM GLOVES-MEDIUM
10850046528016PREVENTI- BIODEGRADABLE POWDER-FREE NITRILE EXAM GLOVES- SMALL
10850046528009PREVENTI- BIODEGRADABLE POWDER-FREE NITRILE EXAM GLOVES-X-SMALL

Trademark Results [PREVENTI]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PREVENTI
PREVENTI
98199638 not registered Live/Pending
Preventi
2023-09-27
PREVENTI
PREVENTI
77142235 not registered Dead/Abandoned
Medtronic, Inc.
2007-03-28
PREVENTI
PREVENTI
76386549 2741260 Dead/Cancelled
Torres, Jose Garcia
2002-03-21
PREVENTI
PREVENTI
73675485 1480703 Dead/Cancelled
A&R MARKETING, INC.
1987-07-30

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