Dreamworks Gabby's Dollhouse

GUDID 60017276238640

Adhesive Bandages, 3/4 IN x 3 IN (19 mm x 76 mm)

Aso LLC

Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial Skin-cover adhesive strip, non-antimicrobial
Primary Device ID60017276238640
NIH Device Record Keyd38659a0-0019-44b2-b20a-da269a196ac5
Commercial Distribution StatusIn Commercial Distribution
Brand NameDreamworks Gabby's Dollhouse
Version Model Number017276238648
Company DUNS152793493
Company NameAso LLC
Device Count14
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Countertrue

Customer Support Contacts

Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx
Phone18558234545
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS100017276238648 [Primary]
GS160017276238640 [Unit of Use]

FDA Product Code

KGXTape And Bandage, Adhesive

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-01-19
Device Publish Date2022-01-11