Acculite™ EndoOcular® - LUMENIS INC.

Duns Number:043618763

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More Product Details

Catalog Number

-

Brand Name

Acculite™ EndoOcular®

Version/Model Number

" Aspirat., 20ga 45° bend, SMA 906, 200µm"

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

August 28, 2019

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

Yes

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

-

Product Code Details

Product Code

HJM

Product Code Name

Transilluminator, Ac-Powered

Device Record Status

Public Device Record Key

42c653db-1891-4936-8f06-5f9578a9b09f

Public Version Date

August 29, 2019

Public Version Number

4

DI Record Publish Date

September 12, 2016

Additional Identifiers

Package DI Number

17290109140756

Quantity per Package

10

Contains DI Package

07290109140759

Package Discontinue Date

September 12, 2016

Package Status

Not in Commercial Distribution

Package Type

-

"LUMENIS INC." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 48