FDA UDI In Commercial Distribution 🇺🇸 United States

Mui Scientific

DI: 10678467003253 · Model: S-R8-1019 · 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
10678467003253
Version / Model
S-R8-1019
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
2018-08-21
Public Version
2
Public Version Date
2022-08-05
Public Version Status
Update
Public Device Record Key
cdd532d2-92cf-4537-bacf-c4dd7e8a8fec

Device Description

CUSTOMIZED SINGLE-USE 8-channel Anorectal Colonic

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
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
Primary 10678467003253
Unit of Use 00678467003256

Customer Contacts

Phone
9058905525

Premarket Submissions

Submission Number Supplement Number
K823701 000