Primary Device ID | 00880304988408 |
NIH Device Record Key | b0e8268c-3c4c-4e92-a925-3a56bb5a92ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Zyston® Strut |
Version Model Number | 100M6101 |
Catalog Number | 100M6101 |
Company DUNS | 018577570 |
Company Name | BIOMET SPINE LLC |
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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00880304988408 [Primary] |
LRP | TRAY, SURGICAL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00880304988408]
Moist Heat or Steam Sterilization
[00880304988408]
Moist Heat or Steam Sterilization
[00880304988408]
Moist Heat or Steam Sterilization
[00880304988408]
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[00880304988408]
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[00880304988408]
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[00880304988408]
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[00880304988408]
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[00880304988408]
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[00880304988408]
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[00880304988408]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-08-09 |
Device Publish Date | 2018-07-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ZYSTON 77945862 4039201 Live/Registered |
ZIMMER BIOMET SPINE, INC. 2010-02-26 |