FDA UDI In Commercial Distribution 🇺🇸 United States

MMS

DI: 05055140703170 · Model: MMS5702 · MEDIPLUS LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
MMS
Primary DI
05055140703170
Version / Model
MMS5702
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
8d04cba8-57d8-4851-872a-00cb152e7595

Device Description

Double lumen catheter, 8fr, latex free

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
KGZ ACCESSORIES, CATHETER

GMDN Terms

Code Name
14307 Urodynamic measurement system

Identifiers

Type ID
Package 15055140703177
Primary 05055140703170

Customer Contacts

Device Sizes

Type Value Unit Text
Length 65.0 Centimeter
Catheter Gauge 8.0 French