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Interface for Varian

FDA UDI

Class II (US FDA UDI)

by Medtec LLC

Identity

Trade Name
Interface for Varian FDA UDI
Generic Name
Indexed-immobilization patient positioning system FDA UDI
Device Name
For use with Universal Couchtop™ (1 Piece) FDA UDI
Model / Reference
MTIL6612 FDA UDI
Description
For use with Universal Couchtop™ (1 Piece) FDA UDI

Identifiers

Catalog Number
MTIL6612 FDA UDI
Primary DI / UDI-DI
00841439106310 FDA UDI
510(k) Number
K973842 FDA UDI
FDA Product Code
IXQ FDA UDI
GMDN Term
Indexed-immobilization patient positioning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Indexed-immobilization patient positioning system

Interface for Varian by Medtec LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Indexed-immobilization patient positioning system.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medtec LLC

Sources (1)

  • FDA UDI debbb2b6-dc3a-4445-ae0d-13b457a6d217 36 fields · synced Jun 8, 2026