FDA UDI In Commercial Distribution 🇺🇸 United States

Mui Scientific

DI: 10678467508246 · Model: S7-E16-1026 · H & A Mui Enterprises Inc
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
Mui Scientific
Primary DI
10678467508246
Version / Model
S7-E16-1026
Company Name
H & A Mui Enterprises Inc
Labeler DUNS
243872611
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2025-04-10
Public Version
2
Public Version Date
2026-03-02
Public Version Status
Update
Public Device Record Key
cb2d64e7-9236-4c36-9d88-802d85911a83

Device Description

Single Use Esophageal 16 Ch Catheter

Device Characteristics

Single Use
No
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
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
FFX System, Gastrointestinal Motility (Electrical)

GMDN Terms

Code Name
17745 Gastrointestinal motility manometric catheter, non-electronic

Identifiers

Type ID
Unit of Use 00678467508249
Primary 10678467508246

Premarket Submissions

Submission Number Supplement Number
K823701 000