Convertible Trocar System

FDA UDI

Class II (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name: Convertible Trocar System FDA UDI
Generic Name: Laparoscopic access cannula, reusable FDA UDI
Device Name: Reusable Blunt Tip Obturator FDA UDI
Model / Reference: C0407 FDA UDI
Description: Reusable Blunt Tip Obturator FDA UDI

Identifiers

Primary DI / UDI-DI: 00607915114282 FDA UDI
FDA Product Code: HET FDA UDI
GCJ FDA UDI
GMDN Term: Laparoscopic access cannula, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 884.1720 FDA UDI
876.1500 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 12 Millimeter FDA UDI
Length — 100 Millimeter FDA UDI

Category: Laparoscopic access cannula, reusable

Convertible Trocar System by Applied Medical Resources Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Also classified as Laparoscopic access cannula, reusable.

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Gimmi — Gimmi GmbH · Class II
BLUEENDO — TROKAMED GmbH · Class II
Millennium — AVALIGN TECHNOLOGIES, Inc. · Class II
AESCULAP — AESCULAP, INC. · Class II

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: Applied Medical Resources Corp.

Sources (1)

FDA UDI c19a0591-637a-4f8f-ac97-c0095dba5f99 35 fields · synced May 31, 2026