← Back to catalogue

Pro Advantage

FDA UDI

Class II (US FDA UDI)

by National Distribution & Contracting, Inc.

Identity

Trade Name
Pro Advantage FDA UDI
Generic Name
Electrocautery system generator, battery-powered FDA UDI
Device Name
Pro Advantage Electrode Tip Dermal Sharp Sterile FDA UDI
Model / Reference
P211050 FDA UDI
Description
Pro Advantage Electrode Tip Dermal Sharp Sterile FDA UDI

Identifiers

Catalog Number
P211050 FDA UDI
Primary DI / UDI-DI
M220P2110505 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrocautery system generator, battery-powered 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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrocautery system generator, battery-powered

Pro Advantage by National Distribution & Contracting, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrocautery system generator, battery-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI a79af45a-aed2-4e57-ad69-9ce03e89269c 35 fields · synced Jun 8, 2026