The Doctor's

GUDID 08711744032579

TD SLEEPZZ NIGHTGUARD 1CT PAD 12

MEDTECH PRODUCTS INC.

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Primary Device ID08711744032579
NIH Device Record Key7603b40d-a739-4821-b435-2849501c0413
Commercial Distribution StatusIn Commercial Distribution
Brand NameThe Doctor's
Version Model Number1030450
Company DUNS060272465
Company NameMEDTECH PRODUCTS INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
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

Customer Support Contacts

Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx
Phone1-800-592-6661
Emailxx@xx.xx

Device Identifiers

Device Issuing AgencyDevice ID
GS108711744032548 [Primary]
GS108711744032579 [Package]
Contains: 08711744032548
Package: Single [1 Units]
In Commercial Distribution

FDA Product Code

OBRMouthguard, Over-The-Counter

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-16
Device Publish Date2020-12-08