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Robotic FloShield/Plus

FDA UDI

Class II (US FDA UDI)

by Minimally Invasive Devices, LLC

Identity

Trade Name
Robotic FloShield/Plus FDA UDI
Generic Name
Endoscope lens cleaner, gas/fluid, single-use FDA UDI
Device Name
FloShield/Plus Robotic Tube Set is an accessory for 8.5mm FloShield Robotic Sheath Assembly but is also compatible with 5mm FloShield and 10mm FloShield systems FDA UDI
Model / Reference
RTS1 FDA UDI
Description
FloShield/Plus Robotic Tube Set is an accessory for 8.5mm FloShield Robotic Sheath Assembly but is also compatible with 5mm FloShield and 10mm FloShield systems FDA UDI

Identifiers

Catalog Number
RTS1 FDA UDI
Primary DI / UDI-DI
00815128020614 FDA UDI
FDA Product Code
GCJ FDA UDI
OCT FDA UDI
GMDN Term
Endoscope lens cleaner, gas/fluid, 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

Category: Endoscope lens cleaner, gas/fluid, single-use

Robotic FloShield/Plus by Minimally Invasive Devices, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope lens cleaner, gas/fluid, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e034c87-f809-4107-87d0-4727b96fac86 36 fields · synced May 31, 2026