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Entriport

FDA UDI

Class II (US FDA UDI)

by Conmed Corporation

Identity

Trade Name
ENTRIPORT FDA UDI
Generic Name
Laparoscopic access cannula anchor, reusable FDA UDI
Device Name
Fascia Anchor Adapter Seal Replacement FDA UDI
Model / Reference
G3-R12GK FDA UDI
Description
Fascia Anchor Adapter Seal Replacement FDA UDI

Identifiers

Catalog Number
G3-R12GK FDA UDI
Primary DI / UDI-DI
20653405082467 FDA UDI
510(k) Number
K142464 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Laparoscopic access cannula anchor, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

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

Cleared under the same submission

K142464 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conmed Corporation

Sources (1)

  • FDA UDI a7cd9fc5-d3c1-4ec0-bc5f-8c327f188a45 39 fields · synced Jun 1, 2026