Welch Allyn, Inc. - Welch Allyn 767 Integrated Wall Diagnostic System - WELCH ALLYN, INC.

Duns Number:198227881

Device Description: Welch Allyn 767 Integrated Wall Diagnostic System including Wall Aneroid Sphygmomanometer Welch Allyn 767 Integrated Wall Diagnostic System including Wall Aneroid Sphygmomanometer (#7670-01), Standard Ophthalmoscope (#11710), MacroView Otoscope (#23810), KleenSpec Disposable Specula Dispenser, Wall-Mount Panel (40 x 12 in / 101.6 x 30.5 cm)

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More Product Details

Catalog Number

76782-M

Brand Name

Welch Allyn, Inc.

Version/Model Number

901027

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 24, 2017

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

-

Product Code Details

Product Code

HMF

Product Code Name

STAND, INSTRUMENT, AC-POWERED, OPHTHALMIC

Device Record Status

Public Device Record Key

7a2d7d23-e570-4f99-b3d0-71f4e55f51d7

Public Version Date

July 22, 2021

Public Version Number

3

DI Record Publish Date

September 17, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"WELCH ALLYN, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 374
2 A medical device with a moderate to high risk that requires special controls. 4080
3 A medical device with high risk that requires premarket approval 1