AHT INC

GUDID 26975913450014

AHT INC

Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator Infrared-light vein locator
Primary Device ID26975913450014
NIH Device Record Key8f1a5e8d-8b43-460f-bfa0-31057e11e2df
Commercial Distribution StatusIn Commercial Distribution
Brand NameAHT INC
Version Model NumberVD80
Company DUNS403440561
Company NameAHT INC
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS126975913450014 [Primary]

FDA Product Code

KZADevice, Vein Location, Liquid Crystal

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-08
Device Publish Date2023-05-31
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