Primary Device ID | B167900051410 |
NIH Device Record Key | 64d957cc-f48c-49d3-a20c-b5adaf7a54a2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CURE LP |
Version Model Number | 9-00051-41 |
Company DUNS | 182698477 |
Company Name | MEDITECH SPINE, LLC |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B167900051410 [Primary] |
KWQ | Appliance, fixation, spinal intervertebral body |
Steralize Prior To Use | true |
Device Is Sterile | false |
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
[B167900051410]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-10-06 |