Primary Device ID | 00811954012663 |
NIH Device Record Key | db4e9b04-6217-4987-9c16-7b24c35033f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | 2.7mm Go-No Go Gauge |
Version Model Number | 6006 |
Catalog Number | 6006 |
Company DUNS | 017663522 |
Company Name | INTERVENTIONAL SPINE, 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 | 800-497-0484 |
www.cs@i-spineinc.com | |
Phone | 800-497-0484 |
www.cs@i-spineinc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00811954012663 [Primary] |
HTJ | Gauge, Depth |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00811954012663]
Moist Heat or Steam Sterilization
[00811954012663]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2015-12-22 |
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