Capture™ 1202-01

GUDID M7831202010

Four Chamber Polyp Trap

DIVERSATEK HEALTHCARE, INC.

General specimen container IVD, no additive, non-sterile General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium General specimen container IVD, no additive/medium
Primary Device IDM7831202010
NIH Device Record Key387eca29-7fbf-47fd-ad54-3ed31b72f70d
Commercial Distribution StatusIn Commercial Distribution
Brand NameCapture™
Version Model Number1202-01
Catalog Number1202-01
Company DUNS030650113
Company NameDIVERSATEK HEALTHCARE, 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 Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com
Phone800-558-6408
Emailsales@diversatekhc.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7831202010 [Primary]
HIBCCM7831202011 [Package]
Package: Case [25 Units]
In Commercial Distribution

FDA Product Code

KDQBottle, Collection, Vacuum

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-04-10
Device Publish Date2016-09-17

Devices Manufactured by DIVERSATEK HEALTHCARE, INC.

M78312011061 - Diversatek Healthcare2024-02-08 Basic Endoscopy Procedure Kit
10816734023355 - BullDog®2023-09-04 Air/Water Channel Cleaning Adapter for Fujifilm® GI Endoscope
00816734023181 - SafeGuide® Single2023-08-22 Disposable Over the Guidewire Esophageal Dilator, 15 FR
00816734023198 - SafeGuide® Single2023-08-22 Disposable Over the Guidewire Esophageal Dilator, 18 FR
00816734023204 - SafeGuide® Single2023-08-22 Disposable Over the Guidewire Esophageal Dilator, 21 FR
00816734023211 - SafeGuide® Single2023-08-22 Disposable Over the Guidewire Esophageal Dilator, 24 FR
00816734023228 - SafeGuide® Single2023-08-22 Disposable Over the Guidewire Esophageal Dilator, 27 FR
00816734023235 - SafeGuide® Single2023-08-22 Disposable Over the Guidewire Esophageal Dilator, 30 FR

Trademark Results [Capture]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CAPTURE
CAPTURE
98432555 not registered Live/Pending
Verikai Inc.
2024-03-04
CAPTURE
CAPTURE
97695445 not registered Live/Pending
Neural DSP Technologies Oy
2022-11-29
CAPTURE
CAPTURE
97550370 not registered Live/Pending
Pittman Dental Laboratory
2022-08-16
CAPTURE
CAPTURE
97549124 not registered Live/Pending
Forward Beauty Inc.
2022-08-15
CAPTURE
CAPTURE
97536516 not registered Live/Pending
CAPTURE COLLECTIVE, INC.
2022-08-05
CAPTURE
CAPTURE
97536444 not registered Live/Pending
CAPTURE COLLECTIVE, INC.
2022-08-05
CAPTURE
CAPTURE
97536344 not registered Live/Pending
CAPTURE COLLECTIVE, INC.
2022-08-05
CAPTURE
CAPTURE
97536238 not registered Live/Pending
CAPTURE COLLECTIVE, INC.
2022-08-05
CAPTURE
CAPTURE
97113068 not registered Live/Pending
Carmen Maxwell A
2021-11-08
CAPTURE
CAPTURE
90976916 not registered Live/Pending
YesVideo, Inc.
2020-09-14
CAPTURE
CAPTURE
90723607 not registered Live/Pending
Ademco Inc.
2021-05-20
CAPTURE
CAPTURE
90317905 not registered Live/Pending
Breg, Inc.
2020-11-13
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