Devon 31142535

GUDID 20884527015792

Micro Tip Wipe

Cardinal Health, Inc.

Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad Electrosurgical tip cleaning pad
Primary Device ID20884527015792
NIH Device Record Keycb316dc9-c19c-4cde-a39b-052fd44035bc
Commercial Distribution StatusIn Commercial Distribution
Brand NameDevon
Version Model Number31142535
Catalog Number31142535
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

Operating and Storage Conditions

Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;
Special Storage Condition, SpecifyBetween 0 and 0 *;

Device Identifiers

Device Issuing AgencyDevice ID
GS110884527015795 [Package]
Contains: 30884527015799
Package: CASE [100 Units]
In Commercial Distribution
GS120884527015792 [Package]
Contains: 30884527015799
Package: PACK_OR_INNER_PACK [25 Units]
In Commercial Distribution
GS130884527015799 [Primary]

FDA Product Code

KDCINSTRUMENT, SURGICAL, DISPOSABLE

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-02-15
Device Publish Date2018-06-23

On-Brand Devices [Devon]

10884527020171Suture Removal Kit,7044 Suture Removal Kit
20884527020154Suture Removal Kit,7042 Suture Removal Kit
10884527020140Suture Removal Kit,7046 Suture Removal Kit
20884527020062Suture Removal Kit,7044-MHH Suture Removal Kit
208845270165461822 Foam Block Needle Counter
208845270165391820 Foam Block Needle Counter
108845270165251812 Foam Block Needle Counter
208845270165081880 Foam Block Needle Counter
208845270164921630 Foam Strip Needle Counter
108845270164711810 Foam Block Needle Counter
108845270164641100 Single Magnet Needle Counter,Black
208845270164541842 Foam Block Needle Counter
208845270164471910 Foam Block Needle Counter
208845270164231920 Foam Block Needle Counter
108845270164191930 Foam Block Needle Counter
108845270164021922 Foam Block Needle Counter
208845270163931960 Foam Block Needle Counter
208845270163171840 Foam Block Needle Counter
208845270162871330 Double Foam Strip Needle Counter
108845270162731614 Foam Strip Needle Counter
208845270162491540 Double Magnet Needle Counter,White
108845270162351105 Foam Strip Needle Counter
208845270162251360 Foam Strip Needle Counter
108845270162111200 Double Magnet Needle Counter,Black
108845270162041315 Foam Strip Needle Counter
108845270161981314 Foam Strip Needle Counter
108845270161811260 Double Magnet Needle Counter,Black
208845270161711230 Double Magnet Needle Counter,Black
108845270161671110 Single Magnet Needle Counter,Black
208845270161571530 Double Magnet Needle Counter,Black
20884527016041Skin Marker,Fine Tip
10884527015962Printed Medication Labels
20884527015952Utility Marker with Preprinted Labels
10884527015917Utility Marker Labels
10884527015900Anti-fog Solution,1910 Needle Counter
10884527015894Scope Adjustment Bag
20884527015884Anti-Fog Solution with Foam Pad
20884527015839Tube Holder,Fixed Touch Fasten Strap
10884527015825Tube Holder,Removable Touch Fasten Strap
20884527015815Blade Shield Scalpel Holder
10884527015801Instrument Pouch,Double Pocket
20884527015792Micro Tip Wipe
20884527011763Light Handle
10884527011742Scope Adjustment Bag
10884527011735Light Glove
20884527011718Light Glove
20884527011701Light Glove
20884527011695Light Handle
10884527011681Light Handle
108845270116297075 Staple Remover

Trademark Results [Devon]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DEVON
DEVON
98278891 not registered Live/Pending
Hines Interests Limited Partnership
2023-11-20
DEVON
DEVON
98188439 not registered Live/Pending
DEVON GUITARS
2023-09-20
DEVON
DEVON
97211388 not registered Live/Pending
DEVCOR CAPITAL INC.
2022-01-10
DEVON
DEVON
88424843 not registered Live/Pending
Cardinal Health 529, LLC
2019-05-10
DEVON
DEVON
85802470 4453636 Live/Registered
ASCENT HEALTHCARE, LLC
2012-12-13
DEVON
DEVON
85382582 not registered Dead/Abandoned
BLACK KNIGHT HOLDINGS, LLC
2011-07-27
DEVON
DEVON
81040117 1040117 Dead/Cancelled
Advanco Inc.
0000-00-00
DEVON
DEVON
79063566 3712283 Dead/Cancelled
CHERVON (CHINA) TRADING CO., LTD.
2008-08-07
DEVON
DEVON
78610143 3076726 Live/Registered
HOULIHAN'S RESTAURANTS, INC.
2005-04-15
DEVON
DEVON
77859791 not registered Dead/Abandoned
Devon Motorworks, LLC
2009-10-28
DEVON
DEVON
77759825 3736845 Live/Registered
Devon Energy Corporation
2009-06-15
DEVON
DEVON
77713354 3783541 Live/Registered
Devon Self Storage Holdings (US) LLC
2009-04-14

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