FDA UDI In Commercial Distribution 🇺🇸 United States

mcompass Anorectal Manometry System

DI: 00851607003051 · Model: RMD-001 · MEDSPIRA, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
mcompass Anorectal Manometry System
Primary DI
00851607003051
Version / Model
RMD-001
Catalog Number
RMD-001
Company Name
MEDSPIRA, LLC
Labeler DUNS
962187964
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-01-06
Public Version
5
Public Version Date
2019-11-08
Public Version Status
Update
Public Device Record Key
0cd4a39c-a42f-4f29-9fad-1d23290216db

Device Description

Medspira mcompass Diagnostic Anorectal Manometry system

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
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
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
35053 Manometric gastrointestinal motility analysis system

Identifiers

Type ID
Package 10851607003058
Primary 00851607003051

Customer Contacts

Phone
612-789-0013

Premarket Submissions

Submission Number Supplement Number
K120088 000