AincA® - Handle, Fiber Optic Lighted Stylet, Replacement, - ANESTHESIA ASSOCIATES, INC.

Duns Number:002065670

Device Description: Handle, Fiber Optic Lighted Stylet, Replacement, w/XB Bulb, Chrome Brass, fits 00-469, 00- Handle, Fiber Optic Lighted Stylet, Replacement, w/XB Bulb, Chrome Brass, fits 00-469, 00-470 (Req 2 AA)

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More Product Details

Catalog Number

00-471

Brand Name

AincA®

Version/Model Number

00-471

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

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

BSR

Product Code Name

STYLET, TRACHEAL TUBE

Device Record Status

Public Device Record Key

64a5c5a0-dc42-49f2-a516-9012540460ce

Public Version Date

April 08, 2021

Public Version Number

1

DI Record Publish Date

March 31, 2021

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ANESTHESIA ASSOCIATES, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 561
2 A medical device with a moderate to high risk that requires special controls. 135