IMCO

GUDID 20815842023155

Facemask, Earloop, Economy, Blue

INDEPENDENT MEDICAL CO-OP, INC.

Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use Surgical/medical face mask, single-use
Primary Device ID20815842023155
NIH Device Record Keyb86aa8f2-6902-4f6e-9fa6-627e408afe33
Commercial Distribution StatusIn Commercial Distribution
Brand NameIMCO
Version Model Number1530-IMC
Company DUNS073436164
Company NameINDEPENDENT MEDICAL CO-OP, INC.
Device Count1
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 Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100815842023151 [Primary]
GS110815842023158 [Package]
Contains: 00815842023151
Package: Inner Pack [50 Units]
In Commercial Distribution
GS120815842023155 [Package]
Contains: 10815842023158
Package: Case [10 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FXXMask, Surgical

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2020-05-06
Device Publish Date2016-06-20

On-Brand Devices [IMCO]

10815842023400Woven Tape Measure
10815842023394Standard Bulb and Valve, LF
20815842023179Sterilization Pouch, SS, 12" x 15"
20815842023162Facemask, Earloop, Economy, Yellow
20815842023155Facemask, Earloop, Economy, Blue
20815842023148Sterilization Pouch, SS, 5 1/4" x 10"
20815842023131Sterilization Pouch, SS, 3 1/2" x 9"
20815842023124Sterilization Pouch, SS, 7 1/2" x 13"
20815842023117Sterilization Pouch, SS, 3 1/2"x 6 1/2"
10815842023103Standard Bulb and Valve
10815842023097Cuff and Bladder, 2 Tube, Large Adult
10815842023080Cuff and Bladder, 2 Tube, Adult
10815842023073Cuff and Bladder, 2 Tube, Small Adult
10815842023066Gauge for Premium and Standard Aneroid
10815842023059Aneroid Sphygmomanometer, Value Line, Adult
10815842023042Aneroid Sphygmomanometer, Value Line, Large Adult
10815842023035Aneroid Sphygmomanometer, Value Line, Child
10815842023028Aneroid Sphygmomanometer, Basic, Large Adult
10815842023011Aneroid Sphygmomanometer, Basic, Small Adult
10815842023004Aneroid Sphygmomanometer, Basic, Adult
10815842022991Aneroid Sphygmomanometer, Standard, Large Adult
10815842022984Aneroid Sphygmomanometer, Standard, Adult
10815842022977Aneroid Sphygmomanometer, Standard, Small Adult
10815842022960Aneroid Sphygmomanometer, Premium, Large Adult
00815842022956Aneroid Sphygmomanometer, Premium, Small Adult
10815842022946Aneroid Sphygmomanometer, Premium, Adult
10815842021604Polyglycolic Suture, 4-0, C3 Needle
10815842021598Poluglycolic Suture, 5-0, C3 Needle
10815842021581Polyglycolic Suture, 4-0, C6 Needle
10815842021574Polypropylene Suture, 4-0, C3 Needle
10815842021567Polypropylene Suture, 5-0, C3 Needle
10815842021550Polypropylene Suture, 6-0, C1 Needle
10815842021543Polypropylene Suture, 4-0, C6 Needle
10815842021536Nylon Suture, 4-0, C3 Needle
10815842021529Nylon Suture, 5-0, C-3 Needle
10815842021512Nylon Suture, 6-0, C1 Needle
10815842021505Nylon Suture, 3-0, C7 Needle
10815842021499Nylon Sutuer, 4-0, C6 Needle
10815842021482Nylon Suture, 5-0, C6 Needle
10815842021475Nylon Suture, 6-0, C3 Needle
00815842021461Nylon Suture, 4-0, PC 31 Needle

Trademark Results [IMCO]

Mark Image

Registration | Serial
Company
Trademark
Application Date
IMCO
IMCO
88112253 5727503 Live/Registered
IMCO General Construction, Inc.
2018-09-11
IMCO
IMCO
87732927 not registered Live/Pending
Raffles Investments (Proprietary) Limited
2017-12-22
IMCO
IMCO
87692780 not registered Dead/Abandoned
Inventory Systems GmbH
2017-11-21
IMCO
IMCO
87437635 not registered Live/Pending
IMCO PARTNERS LTD.
2017-05-04
IMCO
IMCO
86962606 5258731 Live/Registered
Imco Technology, Inc.
2016-04-03
IMCO
IMCO
86937139 5067647 Live/Registered
Inman Marine Corporation
2016-03-11
IMCO
IMCO
79291946 not registered Live/Pending
COGNE ACCIAI SPECIALI S.p.A.
2020-06-24
IMCO
IMCO
79237793 5790497 Live/Registered
Georg HACHMANN
2017-11-28
IMCO
IMCO
79134900 4493170 Live/Registered
Windmill Co., Ltd.
2013-04-25
IMCO
IMCO
78959901 3518490 Live/Registered
IMCO Carbide Tool Inc.
2006-08-24
IMCO
IMCO
78959876 3514340 Live/Registered
IMCO Carbide Tool Inc.
2006-08-24
IMCO
IMCO
78949646 3251759 Live/Registered
Independent Medical Co-Op, Inc.
2006-08-10

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.