Primary Device ID | 00889024335301 |
NIH Device Record Key | 85ec6e1b-5f30-4dc8-b1d0-fc733e9c4d42 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sequoia® |
Version Model Number | 3313-050 |
Catalog Number | 3313-050 |
Company DUNS | 787663400 |
Company Name | ZIMMER SPINE, INC. |
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 |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Length | 50 Millimeter |
Outer Diameter | 5.5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024335301 [Primary] |
MNI | ORTHOSIS, SPINAL PEDICLE FIXATION |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
[00889024335301]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-20 |
Device Publish Date | 2015-09-24 |