Duragold® Reuseable Cannula

FDA UDI

Class II (US FDA UDI)

by Applied Medical Resources Corp.

Identity

Trade Name: Duragold® Reuseable Cannula FDA UDI
Generic Name: Laparoscopic access cannula, reusable FDA UDI
Device Name: Laparoscopic Trocar Sleeve/Reusable FDA UDI
Model / Reference: C0E08 FDA UDI
Description: Laparoscopic Trocar Sleeve/Reusable FDA UDI

Identifiers

Primary DI / UDI-DI: 00607915115623 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Laparoscopic access cannula, reusable 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

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 — 5 Millimeter FDA UDI
Length — 100 Millimeter FDA UDI

Category: Laparoscopic access cannula, reusable

Duragold® Reuseable Cannula 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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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 207cf2e6-1a01-4aaf-91a4-168903264ea8 35 fields · synced Jun 8, 2026