FDA UDI Not in Commercial Distribution 🇺🇸 United States

hi-slip® full plus

DI: 08697749683445 · Model: HS.FPF2010 · 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
hi-slip® full plus
Primary DI
08697749683445
Version / Model
HS.FPF2010
Catalog Number
HS.FPF2010
Company Name
OASIS MEDIKAL URUNLER KIMYA TURIZM SANAYI VE TICARET ANONIM SIRKETI
Labeler DUNS
534998190
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
3
Public Version Date
2022-12-26
Public Version Status
Update
Public Device Record Key
19ef7345-8253-4473-ae33-a827a68ae04c
Distribution End Date
2022-08-01

Device Description

Single Use Hydrophilic Urinary Catheter With Water Sachet And Accessories Fem/Ped 8" 10FR

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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 08697749683049
Primary 08697749683445
Package 08697749687511

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 10 French
Length 8 Inch

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep dry and keep away from sunlight