Primary Device ID | M7249000031 |
NIH Device Record Key | 56046e7c-3ed3-490f-92f0-3bc79a378bd1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 900-003 Bilateral Groove Chin Sizer Set |
Version Model Number | 900-003 |
Catalog Number | 900-003 |
Company DUNS | 784664955 |
Company Name | IMPLANTECH ASSOCIATES, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com | |
Phone | 1-800-733-0833 |
info@implantech.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M7249000031 [Primary] |
FWP | Prosthesis, Chin, Internal |
Steralize Prior To Use | true |
Device Is Sterile | false |
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
[M7249000031]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-07-28 |
Device Publish Date | 2021-07-20 |
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