FDA.reportPublic FDA data

UniTip High Resolution Catheter

Primary DI
07640172974001
Brand
UniTip High Resolution Catheter
Company
Unisensor AG
Model
K8159-00-2101-D
Catalog number
K8159-00-2101-D
Device description
UniTip High Resolution Catheter 8F
Published
2021-10-20
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true

Product Codes#

Code, Name table
CodeName
FFXSystem, Gastrointestinal Motility (Electrical)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FFXSystem, Gastrointestinal Motility (Electrical)Gastroenterology, Urology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K062222000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K062222000UNITIP HIGH RESOLUTION CATHETERUnisensor AG2007-03-15FFX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07640172974001PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
07640172974001076401729740017640172974001

GMDN Terms#

Term, Definition table
TermDefinition
Gastrointestinal manometric catheter, electronicA non-sterile flexible tube with electronic sensors at the distal end intended to be inserted through the nose or rectum into the gastrointestinal (GI) tract to evaluate peristaltic motility anywhere in the GI tract (pharynx, oesophagus, stomach, duodenum, small bowel, colon, and anorectal area) by measuring pressure; it may additionally be intended to measure pH and electrical impedance and contain a lumen. Also known as a GI solid-state sensor catheter, it is intended for proximal connection to an appropriate gastrointestinal motility analysis system, and the acquired data may be used to generate a 3-D image. This is a reusable device intended to be sterilized/cleaned prior to use.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
483298907
Device count
1
Serial number
true
Manufacturing date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07640172974025UniTip High Resolution CatheterK1036A2-E-22082022-11-03
07640172974032UniTip High Resolution CatheterK121159-00-2209-D2022-11-03
07640172972533Latitude CatheterGIM6000D00K194AC-L-15022016-09-19
07640172972564Latitude CatheterGIM6000A00K84AC-L-15012016-09-19
07640172972595Latitude CatheterGIM6000E00K84AC-00-15032016-09-19
07640172974018UniTip High Resolution CatheterK102059-EL-2106-D2022-04-20
07640172973936UniTip High Resolution CatheterK143659-L6-2103-DK143659-L6-2103-D2022-01-19
07640172973998UniTip High Resolution CatheterK81759-E-2017-D K81759-E-2017-D 2022-01-13
07640172973912UniTip CatheterK6604-00-2011-D2021-02-18
07640172973882UniTip High Resolution CatheterK126A2-00-20142021-02-04
07640172973899UniTip High Resolution CatheterK146A2-00-20152021-02-04
07640172973905UniTip High Resolution CatheterK1212A2-00-20162021-02-04
07640172973851UniTip High Resolution CatheterK1412A2-00-20082020-12-07
07640172973868UniTip CatheterK14172-00-20102020-12-07
07640172973875UniTip CatheterK12172-00-2009 2020-12-07
07640172973844UniTip CatheterK104A2-00-20062020-10-27
07640172973837UniTip High Resolution CatheterK121459-L5-1912-D2020-10-09
07640172973813UniTip High Resolution CatheterK1020A1-EL-1911-D2019-11-11
07640172973783UniTip CatheterK14172-00-19062019-06-17
07640172973790UniTip CatheterK12172-00-19072019-06-17

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Primary DI, Brand, Company table
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00816734023433Diversatek HealthcareDIVERSATEK HEALTHCARE, INC.FFX2025-05-16
00816734023440Diversatek HealthcareDIVERSATEK HEALTHCARE, INC.FFX2025-05-16
00816734023457Diversatek HealthcareDIVERSATEK HEALTHCARE, INC.FFX2025-05-16
00816734023464Diversatek HealthcareDIVERSATEK HEALTHCARE, INC.FFX2025-05-16
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