← Back to catalogue

Turbett Surgical

FDA UDI

Class II (US FDA UDI)

by Turbett Surgical, LLC

Identity

Trade Name
Turbett Surgical FDA UDI
Generic Name
Device sterilization/disinfection container, reusable FDA UDI
Device Name
Ground Loader Cart (Includes loading mechanism) FDA UDI
Model / Reference
TS3035 FDA UDI
Description
Ground Loader Cart (Includes loading mechanism) FDA UDI

Identifiers

Primary DI / UDI-DI
00859464007076 FDA UDI
FDA Product Code
FRG FDA UDI
GMDN Term
Device sterilization/disinfection container, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.6850 FDA UDI
Commercial Distribution
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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Device sterilization/disinfection container, reusable

Turbett Surgical by Turbett Surgical, LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI f84f54dd-0916-4e43-b44b-ee034d4b7e1a 33 fields · synced May 30, 2026