FDA UDI In Commercial Distribution 🇺🇸 United States

GentleCathTM

DI: 00768455142682 · Model: 509000 · OASIS MEDIKAL URUNLER KIMYA TURIZM SANAYI VE TICARET ANONIM SIRKETI
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
GentleCathTM
Primary DI
00768455142682
Version / Model
509000
Catalog Number
509000
Company Name
OASIS MEDIKAL URUNLER KIMYA TURIZM SANAYI VE TICARET ANONIM SIRKETI
Labeler DUNS
534998190
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
9110b123-bd93-4c83-bb09-7d413e86e6d8

Device Description

Hydrophilic Intermittent Urinary Catheter With Water Sachet Tiemann 16'' 12FR

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EZD CATHETER, STRAIGHT

GMDN Terms

Code Name
45605 Single-administration urethral catheterization kit, single-use

Identifiers

Type ID
Package 10768455136169
Package 00768455136162
Primary 00768455142682

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 12 French
Length 16 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry