Primary Device ID | 00192896043312 |
NIH Device Record Key | a72ac0e3-9e88-4c1d-894b-90f1a7ab04d8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GROSSMAN AREOLA MARKER |
Version Model Number | 475-917 |
Catalog Number | 475-917 |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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) 821-7496 |
info@sontecinstruments.com |
Length | 40 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896043312 [Primary] |
GAF | SPATULA, SURGICAL, GENERAL & PLASTIC SURGERY |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896043312]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-09-10 |
Device Publish Date | 2018-09-18 |
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