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MARS Scope Holder

FDA UDI

Class II (US FDA UDI)

by Levita Magnetics International Corp.

Identity

Trade Name
MARS Scope Holder FDA UDI
Generic Name
Magnetic surgical manipulation system instrument, external, electric FDA UDI
Device Name
MARS Scope Holder FDA UDI
Model / Reference
DRA002-04 FDA UDI
Description
MARS Scope Holder FDA UDI

Identifiers

Primary DI / UDI-DI
00852342007076 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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Magnetic surgical manipulation system instrument, external, electric

MARS Scope Holder 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

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Manufacturer

Manufacturer
Levita Magnetics International Corp.

Sources (1)

  • FDA UDI 1ff523f3-c54c-4832-8dd7-ff29d34362f0 33 fields · synced May 30, 2026