FDA UDI In Commercial Distribution 🇺🇸 United States

S-Cath™

DI: 05055140701206 · Model: 5759 · MEDIPLUS LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
S-Cath™
Primary DI
05055140701206
Version / Model
5759
Company Name
MEDIPLUS LTD
Labeler DUNS
228480810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-17
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
93f3a13e-5fab-48e9-b97a-9b1ba926e9b6

Device Description

S-Cath™ System - Silicone suprapubic Foley (open tip) catheter, with introducer set, 16Fr. 10cc, 42cm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KOB CATHETER, SUPRAPUBIC (AND ACCESSORIES)

GMDN Terms

Code Name
34924 Suprapubic drainage catheter

Identifiers

Type ID
Package 15055140701203
Primary 05055140701206

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132890 000

Device Sizes

Type Value Unit Text
Length 42.0 Centimeter
Catheter Gauge 16.0 French