Primary Device ID | 08806373581212 |
NIH Device Record Key | 82138e8a-6782-455e-af06-d8f3fbcc4c5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 4CIS® PINEHURST ANTERIOR CERVICAL PLATE SYSTEM |
Version Model Number | 5932-1111 |
Catalog Number | 5932-1111 |
Company DUNS | 687844241 |
Company Name | ALPHANOX CO.,LTD. |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08806373581212 [Primary] |
KWQ | Appliance, Fixation, Spinal Intervertebral Body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
[08806373581212]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2024-10-29 |
Device Publish Date | 2019-01-24 |
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08806373580758 | 4CIS® Pinehurst Drill Guide-Variable |
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