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Flex

FDA UDI

Class II (US FDA UDI)

by Medrobotics Corporation

Identity

Trade Name
Flex FDA UDI
Generic Name
Robotic surgical arm system FDA UDI
Device Name
TO-LX Case Kit Option 3 FDA UDI
Model / Reference
25778 FDA UDI
Description
TO-LX Case Kit Option 3 FDA UDI

Identifiers

Primary DI / UDI-DI
00850190004766 FDA UDI
FDA Product Code
EOB FDA UDI
GMDN Term
Robotic surgical arm system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4760 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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: Robotic surgical arm system

Flex by Medrobotics Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Robotic surgical arm system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a012e6df-3843-4246-9ba6-ae01968d7c33 33 fields · synced May 30, 2026