Ritter - The Ritter 9' Single Ceiling Mount LED Procedure - MIDMARK CORPORATION

Duns Number:005036025

Device Description: The Ritter 9' Single Ceiling Mount LED Procedure Light is intended to be used in medical e The Ritter 9' Single Ceiling Mount LED Procedure Light is intended to be used in medical environments where illumination is required for medical use during external examinations and procedures.

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More Product Details

Catalog Number

255-002

Brand Name

Ritter

Version/Model Number

255-002

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

KZF

Product Code Name

Device, medical examination, ac powered

Device Record Status

Public Device Record Key

59b0509a-0239-406d-a7b4-dbdc9194a602

Public Version Date

February 23, 2021

Public Version Number

5

DI Record Publish Date

May 31, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MIDMARK CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 838
2 A medical device with a moderate to high risk that requires special controls. 544