Entriport

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name: ENTRIPORT FDA UDI
Generic Name: Laparoscopic access cannula, single-use FDA UDI
Device Name: EntriPort Bladeless Optical Trocar, 5 mm x 150 mm FDA UDI
Model / Reference: G3-05L-NB FDA UDI
Description: EntriPort Bladeless Optical Trocar, 5 mm x 150 mm FDA UDI

Identifiers

Catalog Number: G3-05L-NB FDA UDI
Primary DI / UDI-DI: 20653405082009 FDA UDI
510(k) Number: K142464 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Laparoscopic access cannula, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.1500 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

Ethylene Oxide FDA UDI

Dimensions & Sizes

Size: Length — 100 Millimeter FDA UDI
Width — 5 Millimeter FDA UDI

Category: Laparoscopic access cannula, single-use

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

Similar devices

Also classified as Laparoscopic access cannula, single-use.

Busse Hospital Disposables — ROBERT BUSSE & CO., INC. · Class II
DR. POYNTER MC — APPLIED MEDICAL RESOURCES CORP. · Class II
DR.BRIZENDINE LAP CHOLECYSTECTOMY — APPLIED MEDICAL RESOURCES CORP. · Class I
SECQURE Ultimate — SECQURE SURGICAL, CORP. · Class II
Secondary trocar with Gas Port + Additional Cannula without Gas Port — PURPLE SURGICAL INTERNATIONAL LIMITED · Class II
Auto-shield trocar, ribbed cannula — PURPLE SURGICAL INTERNATIONAL LIMITED · Class II
BluView — Unimax Medical Systems Inc. · Class II
Busse Hospital Disposables — ROBERT BUSSE & CO., INC. · Class II

Cleared under the same submission

K142464 also covers:

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

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

Manufacturer

Manufacturer: Conmed Corporation

Sources (1)

FDA UDI a4a5918d-751d-4a9e-ba74-f3c92694b8c0 38 fields · synced May 30, 2026