Primary Device ID | 04260397088074 |
NIH Device Record Key | 81e33afb-ff05-43f7-98b2-3662687722c8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EIT PLIF Implant Pusher |
Version Model Number | PET30200 |
Company DUNS | 313088331 |
Company Name | EIT Emerging Implant Technologies GmbH |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 |
---|---|
GS1 | 04260397088074 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04260397088074]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-11 |
Device Publish Date | 2018-01-09 |
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