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Electro Lube

FDA UDI

Class II (US FDA UDI)

by Key Surgical, LLC

Identity

Trade Name
Electro Lube FDA UDI
Generic Name
Electrosurgical electrode lubricant FDA UDI
Device Name
Electro Lube NXT is an anti-stick solution to prevent tissue sticking and eschar buildup during electrosurgery and has been validated for use with open, minimally invasive, and robotic instruments. FDA UDI
Model / Reference
EL201 FDA UDI
Description
Electro Lube NXT is an anti-stick solution to prevent tissue sticking and eschar buildup during electrosurgery and has been validated for use with open, minimally invasive, and robotic instruments. FDA UDI

Identifiers

Catalog Number
EL201 FDA UDI
Primary DI / UDI-DI
00724995225025 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical electrode lubricant 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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 4 Milliliter FDA UDI

Category: Electrosurgical electrode lubricant

Electro Lube by Key Surgical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical electrode lubricant.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Key Surgical, LLC

Sources (1)

  • FDA UDI 96357809-81c9-4eb1-a2ac-3c26afdd42e1 36 fields · synced May 30, 2026