Primary Device ID | 07640173166788 |
NIH Device Record Key | 3f3fa153-7129-4029-a294-c7a00dbb02f1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Trabis® |
Version Model Number | 015.030.276 |
Company DUNS | 482467792 |
Company Name | coLigne AG |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +41433438000 |
info@coligne.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640173166788 [Primary] |
PLR | Spinal Vertebral Body Replacement Device - Cervical |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07640173166788]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-02-24 |
Device Publish Date | 2018-09-11 |
07640173167051 | flat cage |
07640173167044 | flat cage |
07640173167037 | flat cage |
07640173167020 | flat cage |
07640173167013 | flat cage |
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07640173166894 | flat cage |
07640173166887 | domed cage |
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07640173166856 | domed cage |
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07640173166788 | domed cage |
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