Constellation, ULTRAVIT, Engauge, 25+ - 25+* ULTRAVIT* Vitrectomy Probe Beveled 25+* - Alcon Laboratories, Inc.

Duns Number:008018525

Device Description: 25+* ULTRAVIT* Vitrectomy Probe Beveled 25+* /10,000 CPM

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More Product Details

Catalog Number

-

Brand Name

Constellation, ULTRAVIT, Engauge, 25+

Version/Model Number

8065752415

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"

Yes

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

HQC

Product Code Name

Unit, phacofragmentation

Device Record Status

Public Device Record Key

fc5d1dc7-a2f4-4884-8790-bf470e1fe116

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 29, 2017

Additional Identifiers

Package DI Number

10380657524157

Quantity per Package

6

Contains DI Package

00380657524150

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-

"ALCON LABORATORIES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 250
2 A medical device with a moderate to high risk that requires special controls. 541
3 A medical device with high risk that requires premarket approval 6098