Audi ZAW-093-059

GUDID 10816058012264

Customer Assistance Kit

DC Safety Sales

Medical bag
Primary Device ID10816058012264
NIH Device Record Keyd7a1a4fe-441d-45ef-9b01-0a5a749739c8
Commercial Distribution Discontinuation2023-07-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameAudi
Version Model NumberZAW-093-059
Catalog NumberZAW-093-059
Company DUNS196527949
Company NameDC Safety Sales
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com
Phone(631)750-2400
Emaildebra.restmeyer@dcsafety.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100816058012267 [Primary]
GS110816058012264 [Package]
Contains: 00816058012267
Package: Bag [1 Units]
Discontinued: 2023-07-31
Not in Commercial Distribution
GS130816058012268 [Package]
Package: Case (bagged) [4 Units]
Discontinued: 2023-07-31
Not in Commercial Distribution

FDA Product Code

LRRFirst Aid Kit With Drug

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2023-08-01
Device Publish Date2023-07-13

On-Brand Devices [Audi]

10816058012455First Aid Kit
10816058012264Customer Assistance Kit

Trademark Results [Audi]

Mark Image

Registration | Serial
Company
Trademark
Application Date
AUDI
AUDI
86352729 4875308 Live/Registered
Audi A.G.
2014-07-30
AUDI
AUDI
85466938 4284786 Live/Registered
Audi AG
2011-11-08
AUDI
AUDI
79352011 not registered Live/Pending
AUDI AG
2022-09-09
AUDI
AUDI
79307062 not registered Live/Pending
AUDI AG
2020-10-20
AUDI
AUDI
79170349 5093264 Live/Registered
AUDI AG
2015-05-27
AUDI
AUDI
79170331 4995364 Live/Registered
AUDI AG
2015-05-27
AUDI
AUDI
79163287 4911093 Live/Registered
AUDI AG
2015-02-24
AUDI
AUDI
78351424 2987328 Live/Registered
AUDI A.G.
2004-01-13
AUDI
AUDI
77415958 3790698 Live/Registered
Audi AG
2008-03-07
AUDI
AUDI
76555604 2912419 Live/Registered
Audi A.G.
2003-10-30
AUDI
AUDI
75090951 2083439 Live/Registered
Audi AG
1996-04-04
AUDI
AUDI
75065880 2073484 Live/Registered
Audi AG
1996-03-01

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.