Omnifix® 4616025V-02

GUDID 04046955850839

OMNIFIX 3 ML US

B. BRAUN MEDICAL INC.

General-purpose syringe, single-use
Primary Device ID04046955850839
NIH Device Record Keyf5d34554-b9c5-4309-983e-771fcf38f4f5
Commercial Distribution StatusIn Commercial Distribution
Brand NameOmnifix®
Version Model Number4616025V-02
Catalog Number4616025V-02
Company DUNS002397347
Company NameB. BRAUN MEDICAL INC.
Device Count100
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com
Phone+1(800)227-2862
EmailBBMUS_Service.EmailOrders@bbraun.com

Device Dimensions

Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter
Total Volume3 Milliliter

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight
Special Storage Condition, SpecifyBetween 0 and 0
Special Storage Condition, SpecifyBetween 0 and 0 *Keep dry
Special Storage Condition, SpecifyBetween 0 and 0 *Keep away from sunlight

Device Identifiers

Device Issuing AgencyDevice ID
GS104046955850815 [Unit of Use]
GS104046955850822 [Primary]
GS104046955850839 [Package]
Contains: 04046955850822
Package: Carton [24 Units]
In Commercial Distribution

FDA Product Code

FMFSyringe, piston

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-03-16
Device Publish Date2026-03-08

On-Brand Devices [Omnifix®]

04046964723247Syringe - Omnifix™, Luer Lock
04046964941177PS20LFN 20ML LL SYR & FLTR NDL SET NRFIT
04046964941153PS5LFN 5ML SYR & FILTER NDL SET NRFIT
04046964723285OMNIFIX 50 ML CATHETER US
04046964723261OMNIFIX 50 ML US
0404696345232210 mL LL 21 Ga. x 1-1/2 in.
04046955607815OMNIFIX 2ML LL LDS,DISPLACEMENT SPIKE-US
04046955292011OMNIFIX 1 ML LL LDS FINE DOSAGE US
04046955850839OMNIFIX 3 ML US

Trademark Results [Omnifix]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OMNIFIX
OMNIFIX
88310707 not registered Live/Pending
Carl Zeiss Industrielle Messtechnik GmbH
2019-02-21
OMNIFIX
OMNIFIX
85638392 4295065 Live/Registered
Omni Materials, Inc.
2012-05-30
OMNIFIX
OMNIFIX
85085311 3928455 Live/Registered
Didax, Incorporated
2010-07-15
OMNIFIX
OMNIFIX
77488451 3781845 Live/Registered
B. Braun Medical Inc.
2008-06-02
OMNIFIX
OMNIFIX
76230619 2809715 Live/Registered
Paul Hartmann AG
2001-03-23
OMNIFIX
OMNIFIX
75293096 2186884 Dead/Cancelled
B. BRAUN MEDICAL INC.
1997-05-16
OMNIFIX
OMNIFIX
74724154 1990071 Dead/Cancelled
AN-CON GENETICS, INC.
1995-08-18
OMNIFIX
OMNIFIX
74562135 2056556 Dead/Cancelled
Philip & Tacey Limited
1994-08-17
OMNIFIX
OMNIFIX
73743585 1539913 Dead/Cancelled
XENETICS BIOMEDICAL, INC.
1988-08-01

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