Primary Device ID | 00842092182154 |
NIH Device Record Key | 98059ad3-61f5-42d2-964e-fc825ecb8914 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Equator |
Version Model Number | 2149104 |
Catalog Number | 2149104 |
Company DUNS | 117776048 |
Company Name | Preat Corporation |
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) 232-7732 |
info@preat.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00842092182154 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00842092182154]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-19 |
Device Publish Date | 2024-02-09 |
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