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Penadapt

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
PENADAPT FDA UDI
Generic Name
Surgical plume evacuation system tube FDA UDI
Device Name
PenAdapt Electrosurgical Pencil Adapter 10 ft (30.5 m) tubing FDA UDI
Model / Reference
PA2010BCB FDA UDI
Description
PenAdapt Electrosurgical Pencil Adapter 10 ft (30.5 m) tubing FDA UDI

Identifiers

Catalog Number
PA2010BCB FDA UDI
Primary DI / UDI-DI
20845854080792 FDA UDI
FDA Product Code
FYD FDA UDI
GMDN Term
Surgical plume evacuation system tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.5070 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
Sterilization Method
Radiation Sterilization FDA UDI

Category: Surgical plume evacuation system tube

Penadapt by Conmed Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical plume evacuation system tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 4f1c4cf3-6794-49ab-bd6b-5cc31f0a3de9 35 fields · synced Jun 8, 2026