Primary Device ID | 00811954012977 |
NIH Device Record Key | 0c26d0da-96aa-40ba-85b3-7d4e4d0193cb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Large Quick Connect Handle |
Version Model Number | 6033 |
Catalog Number | 6033 |
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 | 00811954012977 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00811954012977]
Moist Heat or Steam Sterilization
[00811954012977]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2015-12-22 |
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