← Back to catalogue

Entriport

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ENTRIPORT FDA UDI
Generic Name
Laparoscopic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
EntriPort Reposable, Bladeless Optical Trocar, 7/8 mm x 100 mm FDA UDI
Model / Reference
G3-08-RNB FDA UDI
Description
EntriPort Reposable, Bladeless Optical Trocar, 7/8 mm x 100 mm FDA UDI

Identifiers

Catalog Number
G3-08-RNB FDA UDI
Primary DI / UDI-DI
20653405082160 FDA UDI
510(k) Number
K142464 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic surgical procedure kit, non-medicated, 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

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
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Length — 100 Millimeter FDA UDI
Width — 0.875 Millimeter FDA UDI

Category: Laparoscopic surgical procedure kit, non-medicated, single-use

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

Similar devices

Also classified as Laparoscopic surgical procedure kit, non-medicated, single-use.

Cleared under the same submission

K142464 also covers:

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

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI 1cde0136-25a4-4de2-afa7-796cb9cc1e80 38 fields · synced Jun 1, 2026