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Leadwire Set for CS6101 Stimulator

FDA UDI

Class II (US FDA UDI)

by Control Solutions, Inc.

Identity

Trade Name
Leadwire Set for CS6101 Stimulator FDA UDI
Generic Name
Physical therapy ultrasound/neuromuscular stimulation system FDA UDI
Device Name
CS2110B Cable Set, Concentric to Dual Electrodes FDA UDI
Model / Reference
CS2110B Cable Set, Concentric to Dual Electrodes FDA UDI
Description
CS2110B Cable Set, Concentric to Dual Electrodes FDA UDI

Identifiers

Primary DI / UDI-DI
00860009424777 FDA UDI
FDA Product Code
LIH FDA UDI
QPL FDA UDI
GMDN Term
Physical therapy ultrasound/neuromuscular stimulation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5890 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

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Physical therapy ultrasound/neuromuscular stimulation system

Leadwire Set for CS6101 Stimulator by Control Solutions, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Physical therapy ultrasound/neuromuscular stimulation system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 64e0f96f-5493-41a2-8c44-2183d089eb2e 33 fields · synced May 30, 2026