FDA.reportPublic FDA data

GentleCathTM

Primary DI
07333387044019
Brand
GentleCathTM
Company
OASIS MEDIKAL URUNLER KIMYA TURIZM SANAYI VE TICARET ANONIM SIRKETI
Model
509007
Catalog number
509007
Device description
Hydrophilic Intermittent Urinary Catheter With Water Sachet And Insertion Kit Female 8'' 14FR
Published
2024-06-01
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LYZVinyl patient examination glove

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LYZVinyl Patient Examination GloveGeneral Hospital1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
07333387044019PackageGS110In Commercial Distribution
07333387044026PackageGS14In Commercial Distribution
00768455142750PreviousGS10
07333387044002PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
07333387044019073333870440197333387044019
07333387044026073333870440267333387044026
00768455142750007684551427507684551427500768455142750
07333387044002073333870440027333387044002

GMDN Terms#

Term, Definition table
TermDefinition
Single-administration urethral catheterization kit, single-useA sterile collection of devices that includes a urological catheter (with or without a urine drainage bag), a cap, and other related accessories intended for one-time, self-urinary catheterization. The catheter is inserted through the urethra by the patient to provide urine drainage. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Catheter Gauge14French
Length8Inch

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Keep dry

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+1(800)422-8818cic@convatec.com

Regulatory Flags#

DUNS number
534998190
Device count
1
DM exempt
true
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00768455142576GentleCathTM5089895089892016-09-23
00768455142583GentleCathTM5089905089902016-09-23
00768455142590GentleCathTM5089915089912016-09-23
00768455142606GentleCathTM5089925089922016-09-23
00768455142637GentleCathTM5089955089952016-09-23
00768455142644GentleCathTM5089965089962016-09-23
00768455142651GentleCathTM5089975089972016-09-23
00768455142668GentleCathTM5089985089982016-09-23
00768455142675GentleCathTM5089995089992016-09-23
00768455142682GentleCathTM5090005090002016-09-23
00768455142699GentleCathTM5090015090012016-09-23
00768455142705GentleCathTM5090025090022016-09-23
00768455142712GentleCathTM5090035090032016-09-23
00768455142729GentleCathTM5090045090042016-09-23
00768455142736GentleCathTM5090055090052016-09-23
00768455142743GentleCathTM5090065090062016-09-23
00768455142750GentleCathTM5090075090072016-09-23
00768455142767GentleCathTM5090085090082016-09-23
00768455142774GentleCathTM5090095090092016-09-23
00768455142781GentleCathTM5090105090102016-09-23

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