Primary Device ID | 07640164848334 |
NIH Device Record Key | 6dc29a60-3c15-43b2-bea3-80688bbe33e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | icotec Lumbar Cage PLIF 4° / 25 mm x 10 mm |
Version Model Number | 13-59-42510 |
Catalog Number | 13-59-42510 |
Company DUNS | 480789465 |
Company Name | icotec AG |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
OTC Over-The-Counter | false |
Phone | +41717570000 |
info@icotec.ch |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640164848334 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-08-16 |
Device Publish Date | 2018-07-16 |
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