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OmnisEMG

FDA UDI

Class II (US FDA UDI)

by Accelerated Care Plus Corp.

Identity

Trade Name
OmnisEMG FDA UDI
Generic Name
Biomechanical function analysis/interactive rehabilitation system FDA UDI
Device Name
Biomechanical function analysis / interactive rehabilitation system FDA UDI
Model / Reference
44144 FDA UDI
Description
Biomechanical function analysis / interactive rehabilitation system FDA UDI

Identifiers

Primary DI / UDI-DI
B179OMNI13E87E4 FDA UDI
FDA Product Code
HCC FDA UDI
GMDN Term
Biomechanical function analysis/interactive rehabilitation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Biomechanical function analysis/interactive rehabilitation system

OmnisEMG by Accelerated Care Plus Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biomechanical function analysis/interactive rehabilitation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Accelerated Care Plus Corp.

Sources (1)

  • FDA UDI b708bd16-e382-4bf0-a6bc-e9fa4c9c5319 34 fields · synced May 30, 2026