FDA UDI In Commercial Distribution 🇺🇸 United States

Mediplus

DI: 05055140701343 · Model: 5762 · MEDIPLUS LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mediplus
Primary DI
05055140701343
Version / Model
5762
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
9
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
b98d725e-50e5-47e2-acc3-6d627e5fdb6c

Device Description

Silicone 2 way Foley catheter, 12Fr, standard

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
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
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Package 15055140701340
Primary 05055140701343

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K132890 000

Device Sizes

Type Value Unit Text
Length 42.0 Centimeter
Catheter Gauge 12.0 French