FDA UDI In Commercial Distribution 🇺🇸 United States

OmniME

DI: 00858703006320 · Model: 100MTS · ACCELERATED CARE PLUS CORP
Product Codes
1
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OmniME
Primary DI
00858703006320
Version / Model
100MTS
Company Name
ACCELERATED CARE PLUS CORP
Labeler DUNS
828331616
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-17
Public Version
1
Public Version Date
2023-08-25
Public Version Status
New
Public Device Record Key
adca2900-8801-40d4-9a99-79ff782d11b5

Device Description

Multi-exercise respiratory therapy device with OmniFlow software and sensor, and Synchrony software, electrodes, and sensing devices

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
Yes
Has Serial Number
Yes
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
ION Exerciser, Non-Measuring

GMDN Terms

Code Name
47541 Bioelectrical signal analysis software
63312 Biomechanical function analysis/interactive rehabilitation system
61544 Monitoring spirometer, mechanical

Identifiers

Type ID
Primary 00858703006320

Customer Contacts

Phone
800-350-1100