FloShield 10mm Conical Blunt Obturator

FDA UDI

Class II (US FDA UDI)

by Minimally Invasive Devices, LLC

Identity

Trade Name: FloShield 10mm Conical Blunt Obturator FDA UDI
Generic Name: Laparoscopic trocar blade, reusable FDA UDI
Device Name: The reusable FloShield 10mm Endoscopic Cannula and Blunt Obturator is an access device indicated for use with a disposable 8.5 – 13mm Cannula Seal manufactured by Applied Medical to provide a passageway for the introduction of endoscopic instruments in general laparoscopic procedures. The access device is compatible with the da Vinci Si Surgical System. FDA UDI
Model / Reference: FRT-10D FDA UDI
Description: The reusable FloShield 10mm Endoscopic Cannula and Blunt Obturator is an access device indicated for use with a disposable 8.5 – 13mm Cannula Seal manufactured by Applied Medical to provide a passageway for the introduction of endoscopic instruments in general laparoscopic procedures. The access device is compatible with the da Vinci Si Surgical System. FDA UDI

Identifiers

Catalog Number: FRT-10D FDA UDI
Primary DI / UDI-DI: 00815128020683 FDA UDI
FDA Product Code: GCJ FDA UDI
GMDN Term: Laparoscopic trocar blade, 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

Category: Laparoscopic trocar blade, reusable

FloShield 10mm Conical Blunt Obturator by Minimally Invasive Devices, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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: Minimally Invasive Devices, LLC

Sources (1)

FDA UDI 833596e8-d4c4-4266-bc4c-96efcc1ccc4b 35 fields · synced May 30, 2026