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Canady Plasma GIT Side Fire Probe

FDA UDI

Class II (US FDA UDI)

by Us Medical Innovations, Llc

Identity

Trade Name
Canady Plasma GIT Side Fire Probe FDA UDI
Generic Name
Inert gas-enhanced endoscopic electrosurgical electrode, single-use FDA UDI
Device Name
The Canady Hybrid Plasma GIT probe is an electrosurgical plasma probe that is 2.3mm in diameter and 3.4m long. The electrosurgical plasma probe is used to coagulate biological tissue. FDA UDI
Model / Reference
AW-422541 FDA UDI
Description
The Canady Hybrid Plasma GIT probe is an electrosurgical plasma probe that is 2.3mm in diameter and 3.4m long. The electrosurgical plasma probe is used to coagulate biological tissue. FDA UDI

Identifiers

Primary DI / UDI-DI
B413AW4225410 FDA UDI
510(k) Number
K052035 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Inert gas-enhanced endoscopic electrosurgical electrode, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Inert gas-enhanced endoscopic electrosurgical electrode, single-use

Canady Plasma GIT Side Fire Probe by Us Medical Innovations, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Inert gas-enhanced endoscopic electrosurgical electrode, single-use.

Cleared under the same submission

K052035 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Us Medical Innovations, Llc

Sources (1)

  • FDA UDI 1b755d64-1792-43c4-9032-11883736429e 34 fields · synced Jun 8, 2026