FDA UDI In Commercial Distribution 🇺🇸 United States

Mui Scientific

DI: 00678467508164 · Model: CR1B · H & A Mui Enterprises Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Mui Scientific
Primary DI
00678467508164
Version / Model
CR1B
Company Name
H & A Mui Enterprises Inc
Labeler DUNS
243872611
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-12-02
Public Version
1
Public Version Date
2024-12-10
Public Version Status
New
Public Device Record Key
bf50073f-3f3a-4f79-9249-74cb2fbc3995

Device Description

Reusable PVC Manometric Catheter (Anorectal Balloon Expulsion - Air Only)

Device Characteristics

Single Use
No
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
No
Has Manufacturing Date
Yes
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 00678467508164

Customer Contacts

Phone
905-890-5525

Premarket Submissions

Submission Number Supplement Number
K823701 000