FDA UDI In Commercial Distribution 🇺🇸 United States

Mediplus

DI: 05055140700520 · Model: 2273 · MEDIPLUS LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Mediplus
Primary DI
05055140700520
Version / Model
2273
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
4
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
e2d89531-a3a7-4ea9-86c8-c490f678103b

Device Description

8 channel antroduodenal catheter, 3.9mm

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
No
Sterilization Prior Use
No

Product Codes

Code Name
KLA MONITOR, ESOPHAGEAL MOTILITY, AND TUBE

GMDN Terms

Code Name
17745 Gastrointestinal motility manometric catheter, non-electronic

Identifiers

Type ID
Package 15055140700527
Primary 05055140700520

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K013704 000

Device Sizes

Type Value Unit Text
Length 200.0 Centimeter
Outer Diameter 3.9 Millimeter