FDA UDI In Commercial Distribution 🇺🇸 United States

Mediplus

DI: 05055140701442 · Model: 9111 · MEDIPLUS LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mediplus
Primary DI
05055140701442
Version / Model
9111
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
d7b5d9ba-c5fb-43d7-8760-9d9b8331a594

Device Description

Twin Extension set, 100cm long

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
44675 Urological pressure monitoring tubing set

Identifiers

Type ID
Package 15055140701449
Primary 05055140701442

Customer Contacts

Device Sizes

Type Value Unit Text
Length 100.0 Centimeter
Outer Diameter 3.1 Millimeter
Lumen/Inner Diameter 1.5 Millimeter