Universal Couchtop™ - For IBA L-Series with Lok-Bar™ - MEDTEC, INC.

Duns Number:103977526

Device Description: For IBA L-Series with Lok-Bar™

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More Product Details

Catalog Number

MTIL684115

Brand Name

Universal Couchtop™

Version/Model Number

MTIL684115

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K180021

Product Code Details

Product Code

IXQ

Product Code Name

Table, radiographic, stationary top

Device Record Status

Public Device Record Key

6c6e061c-0ad4-44fb-8f6e-825f6f96e231

Public Version Date

January 08, 2021

Public Version Number

2

DI Record Publish Date

June 18, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MEDTEC, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 31
2 A medical device with a moderate to high risk that requires special controls. 1027