Welch Allyn, Inc. - Welch Allyn SureTemp Plus 692 Wall-Mount - WELCH ALLYN, INC.

Duns Number:198227881

Device Description: Welch Allyn SureTemp Plus 692 Wall-Mount Electronic Thermometer with 4-6 Second Oral, 10-1 Welch Allyn SureTemp Plus 692 Wall-Mount Electronic Thermometer with 4-6 Second Oral, 10-13 Second Rectal and Pediatric Axillary, and 12-15 Second Adult Axillary Temperature Readings in Fahrenheit or Celsius; Interchangeable Oral Probe Well, Oral Probe with 9.0 ft/2.7 m Cord, Last Temperature Recall, 60-Second Pulse/Respiration Timer, Backlit Display with Electronic ID, Anti-Theft Security System; 3 Alkaline AA Batteries; Multiple Language

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More Product Details

Catalog Number

01692-500

Brand Name

Welch Allyn, Inc.

Version/Model Number

901053

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)

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

FLL

Product Code Name

Thermometer, electronic, clinical

Device Record Status

Public Device Record Key

45860a2e-4421-40c3-bdd3-4abb4dfe3681

Public Version Date

June 27, 2022

Public Version Number

6

DI Record Publish Date

December 05, 2017

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