FDA UDI In Commercial Distribution 🇺🇸 United States

Mediplus

DI: 05055140702197 · Model: 5724Y · MEDIPLUS LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mediplus
Primary DI
05055140702197
Version / Model
5724Y
Company Name
MEDIPLUS LTD
Labeler DUNS
228480810
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-16
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
69733091-1611-447a-84a4-763228c640d7

Device Description

Double lumen UPP catheter, 6fr, with Y connector

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
Yes
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
FEN DEVICE, CYSTOMETRIC, HYDRAULIC

GMDN Terms

Code Name
14307 Urodynamic measurement system

Identifiers

Type ID
Package 15055140702194
Primary 05055140702197

Customer Contacts

Device Sizes

Type Value Unit Text
Catheter Gauge 6.0 French
Length 65.0 Centimeter