FDA UDI In Commercial Distribution 🇺🇸 United States

System, mcompass®, Anorectal Manometry

DI: 00851607003457 · Model: RMD-201 · MEDSPIRA, LLC
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
System, mcompass®, Anorectal Manometry
Primary DI
00851607003457
Version / Model
RMD-201
Company Name
MEDSPIRA, LLC
Labeler DUNS
962187964
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-10-06
Public Version
1
Public Version Date
2023-10-16
Public Version Status
New
Public Device Record Key
0cbc2d3a-f8bf-48ee-b4bd-75340dd1f3ea

Device Description

System, mcompass®, Anorectal Manometry

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
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
KLA Monitor, Esophageal Motility, Anorectal Motility, And Tube

GMDN Terms

Code Name
35053 Manometric gastrointestinal motility analysis system
17781 Rectosphincteric balloon

Identifiers

Type ID
Package 10851607003454
Primary 00851607003457

Customer Contacts

Phone
612-789-0013

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Product should be kept dry
Type
Handling Environment Temperature
Temperature Range
2 – 25 Degrees Celsius