900-014 Profile Malar Sizer Set 900-014

GUDID M7249000141

Malar Sizer Set

IMPLANTECH ASSOCIATES, INC.

Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis Malar prosthesis
Primary Device IDM7249000141
NIH Device Record Key3380543f-4c08-4275-9c49-8f324c42810a
Commercial Distribution StatusIn Commercial Distribution
Brand Name900-014 Profile Malar Sizer Set
Version Model Number900-014
Catalog Number900-014
Company DUNS784664955
Company NameIMPLANTECH ASSOCIATES, 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 Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com
Phone1-800-733-0833
Emailinfo@implantech.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7249000141 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

FZEProsthesis, Nose, Internal

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


[M7249000141]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-07-28
Device Publish Date2021-07-20

Devices Manufactured by IMPLANTECH ASSOCIATES, INC.

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