← Back to catalogue

MARS Surgeon Controlled Arm

FDA UDI

Class II (US FDA UDI)

by Levita Magnetics International Corp.

Identity

Trade Name
MARS Surgeon Controlled Arm FDA UDI
Generic Name
Magnetic surgical manipulation system instrument, external, electric FDA UDI
Device Name
MARS Surgeon Controlled Arm FDA UDI
Model / Reference
DRA002 FDA UDI
Description
MARS Surgeon Controlled Arm FDA UDI

Identifiers

Primary DI / UDI-DI
00852342007038 FDA UDI
FDA Product Code
PNL FDA UDI
GMDN Term
Magnetic surgical manipulation system instrument, external, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4815 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Magnetic surgical manipulation system instrument, external, electric

MARS Surgeon Controlled Arm by Levita Magnetics International Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic surgical manipulation system instrument, external, electric.

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

Manufacturer
Levita Magnetics International Corp.

Sources (1)

  • FDA UDI c67e8646-3383-4e4b-8864-6a3393650030 33 fields · synced May 30, 2026