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: PA2010B FDA UDI
Description: PenAdapt Electrosurgical Pencil Adapter 10 ft (30.5 m) tubing FDA UDI

Identifiers

Catalog Number: PA2010B FDA UDI
Primary DI / UDI-DI: 20845854080785 FDA UDI
510(k) Number: K230547 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

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.

Valleylab — Covidien LP · Class II
BCL Accessories Kit — CairnSurgical Inc · Class IIb
Surgimedics® — COASTAL LIFE TECHNOLOGIES, INC. · Class I
SUSI® — Aesculap AG · Class IIa
Gynex — GYNEX CORPORATION · Class I
Smoke Tubing — I.C. Medical, Inc. · Class II
STERILE SURGICAL SCISSORS — Anhui Medfaith Medical Devices Co., Ltd. · Class I
Bovie — BOVIE MEDICAL CORPORATION · Class II

Cleared under the same submission

K230547 also covers:

SnapEvac — Conmed Corporation

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Conmed Corporation

Sources (1)

FDA UDI 05ff1d40-b640-4db0-9b64-db71fa8357ac 36 fields · synced May 30, 2026