FDA UDI In Commercial Distribution 🇺🇸 United States

System, mcompass®, ARM + Biofeedback

DI: 00851607003488 · Model: RMD-203 · MEDSPIRA, LLC
Product Codes
1
GMDN Terms
2
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
System, mcompass®, ARM + Biofeedback
Primary DI
00851607003488
Version / Model
RMD-203
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
029512d8-edb3-4d61-93c2-e79b651c91ed

Device Description

System, mcompass®, ARM + Biofeedback

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 10851607003485
Primary 00851607003488

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