Kendall 55599BG

GUDID 20884521551166

Gentle Border Foam Sacrum

Cardinal Health, Inc.

Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial
Primary Device ID20884521551166
NIH Device Record Key716339c8-192a-4cf0-a996-44f3d9cda1c5
Commercial Distribution StatusIn Commercial Distribution
Brand NameKendall
Version Model Number55599BG
Catalog Number55599BG
Company DUNS080935429
Company NameCardinal Health, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com
Phone+1(508)261-8000
Emailcovidien.udi@covidien.com

Device Dimensions

Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch
Device Size Text, specify0
Length9.25 Inch
Width9.25 Inch

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT
Special Storage Condition, SpecifyBetween 0 and 0 *No;AVOID DIRECT SUNLIGHT

Device Identifiers

Device Issuing AgencyDevice ID
GS110884521551169 [Primary]
GS120884521551166 [Package]
Contains: 10884521551169
Package: PACK_OR_INNER_PACK [10 Units]
In Commercial Distribution
GS130884521551163 [Package]
Contains: 10884521551169
Package: CASE [50 Units]
In Commercial Distribution

FDA Product Code

NADDressing, wound, occlusive

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2021-07-22
Device Publish Date2018-06-30

On-Brand Devices [Kendall]

00884521152765Antimicrobial Bandage Roll
00884521152185Antimicrobial Gauze Sponges
20884521168678Fluff Underpad,X-Large,Moderate
00884521167066Foam Border Gentle Adhesion,6 Inch x 6 Inch (15.2 cm x 15.2 cm) Pad
00884521167004Foam Border Gentle Adhesion,4 Inch x 4 Inch (10.2 cm x 10.2 cm) Pad
00884521166953Foam Border Gentle Adhesion,2 Inch x 4 Inch (5.1 cm x 10.2 cm) Pad
00884521166908Foam Border Gentle Adhesion,2 Inch x 2 Inch (5.1 cm x 5.1 cm) Pad
00884521166830Foam Border Gentle Adhesion,1 Inch x 1-3/4 Inch (2.5 cm x 4.4 cm) Pad
00884521157159Stretch Bandage
00884521157128Stretch Bandage
00884521157104Stretch Bandage
00884521152154Bandage Roll
00884521170783Bandage Roll
00884521153069Antimicrobial Non-adherent Pad
00884521170790Antimicrobial Non-adherent Pad
00884521152833Antimicrobial Adhesive Bandage
00884521152741Antimicrobial Non-adherent Island Dressing
00884521195939Alcohol Prep
00884521065904AMD Antimicrobial Fenestrated Foam Dressing with Top Sheet,0.5% Polyhexamethylene Biguanide HCI
00884521020880Hydrophilic Foam Plus Dressing,Fenestrated
908845211481363000 Isolation Chamber,Rectal
908845211481123100C Apnea Products
108845270047377305 Foam Electrodes,Conductive Adhesive Hydrogel
20884521057941Hydrogel Wound Dressing,Disc
20884521024097Alginate Hydrocolloid Dressing,Border
30884521021918Hydrogel Impregnated Gauze,USP Type VII Gauze Pad 0.25 oz (7 mL) Gel
50884521020960Hydrophilic Foam Island Dressing,4 inch x 4 inch (10.2 cm x 10.2 cm) Pad
20884521007540Transparent Film Dressing,Moisture Vapor Permeable
20884527021793DL Disposable Cable and Lead Wire System,5 Lead Dual Connect, Adapter Required
20884527021786DL Disposable Cable and Lead Wire System
20884527021779DL Disposable Cable and Lead Wire System
10884527021765DL Disposable Cable and Lead System
10884527021758DL Disposable Lead System
10884527021741DL Disposable Lead System
20884527021731DL Disposable Lead System
10884527021727DL Disposable Direct Connect
20884527021717DL Disposable Direct Connect
20884527021700DL Disposable Chest Leads
10884527021697DL Disposable Cable and Lead Wire System,10 Lead, Adapter Required
20884527021687DL Disposable Cable and Lead Wire System,5 Lead, Adapter Required
10884527021673DL Disposable Cable and Lead Wire System,3 Lead, Adapter Required
20884527017284Ultrasound Gel Bottle
3088452701560720661 Adult Multi-Function Defibrillation Electrodes,Radiotransparent
10884527007875Wet Gel Electrodes,GC-11 Foam
108845270078514603 Cloth Wet Gel Electrodes
20884527005878530 Foam Electrodes,Conductive Adhesive Hydrogel
20884527004901Intrauterine Pressure Catheter,Transducer Tipped, Dual Lumen
10884527004874SF450 Foam Electrodes,Conductive Adhesive Hydrogel
10884527004843AC303 Cloth Electrodes,Repositionable, Conductive Adhesive Hydrogel
20884527004833H69P Cloth Electrodes,Repositionable, Conductive Adhesive Hydrogel

Trademark Results [Kendall]

Mark Image

Registration | Serial
Company
Trademark
Application Date
KENDALL
KENDALL
90591223 not registered Live/Pending
SHENZHEN FZONE TECHNOLOGY CO LIMITED
2021-03-19
KENDALL
KENDALL
88660378 not registered Live/Pending
Bemis Manufacturing Company
2019-10-18
KENDALL
KENDALL
88413516 not registered Live/Pending
Kendall Jenner, Inc.
2019-05-02
KENDALL
KENDALL
87082661 5292342 Live/Registered
Phillips 66 Company
2016-06-24
KENDALL
KENDALL
86764949 not registered Dead/Abandoned
AMERICAN GIRL, LLC
2015-09-22
KENDALL
KENDALL
86584671 5138125 Live/Registered
Kendall Jenner, Inc.
2015-04-01
KENDALL
KENDALL
86584660 4999443 Live/Registered
Kendall Jenner, Inc.
2015-04-01
KENDALL
KENDALL
86069210 4587484 Live/Registered
Covidien LP
2013-09-19
KENDALL
KENDALL
85782377 5027358 Live/Registered
KPR U.S., LLC
2012-11-19
KENDALL
KENDALL
85401641 not registered Dead/Abandoned
Abercrombie & Fitch Trading Co.
2011-08-18
KENDALL
KENDALL
85335914 4117666 Live/Registered
Kendall Electric, Inc.
2011-06-02
KENDALL
KENDALL
85203751 4328702 Live/Registered
KPR U.S., LLC
2010-12-22

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