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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 handpiece FDA UDI
Device Name
Pro Advantage Sheath Handpiece Non-sterile FDA UDI
Model / Reference
P211099 FDA UDI
Description
Pro Advantage Sheath Handpiece Non-sterile FDA UDI

Identifiers

Catalog Number
P211099 FDA UDI
Primary DI / UDI-DI
M220P2110993 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrocautery system handpiece 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

Category: Electrocautery system handpiece

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 handpiece.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6aa4772f-aaf7-49e4-b033-8f56766df29d 35 fields · synced Jun 6, 2026