Primary Device ID | 03613720193586 |
NIH Device Record Key | f1177da8-6914-45d3-ba63-f6a7d7f7288a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IMPIX ALIF D |
Version Model Number | B15121212 |
Catalog Number | B15121212 |
Company DUNS | 383228632 |
Company Name | MEDICREA INTERNATIONAL |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03613720193586 [Primary] |
MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-08-06 |
Device Publish Date | 2015-10-24 |
03613720193678 | IMPIX-ALIF D 18mm at 12° |
03613720193654 | IMPIX-ALIF D 18mm at 6° |
03613720193647 | IMPIX-ALIF D 16mm at 12° |
03613720193630 | IMPIX-ALIF D 16mm at 9° |
03613720193623 | IMPIX-ALIF D 16mm at 6° |
03613720193616 | IMPIX-ALIF D 14mm at 12° |
03613720193609 | IMPIX-ALIF D 14mm at 9° |
03613720193593 | IMPIX-ALIF D 14mm at 6° |
03613720193586 | IMPIX-ALIF D 12mm at 12° |
03613720193579 | IMPIX-ALIF D 12mm at 9° |
03613720193562 | IMPIX-ALIF D 12mm at 6° |
03613720193555 | IMPIX-ALIF D 10mm at 12° |
03613720193548 | IMPIX-ALIF D 10mm at 9° |
03613720193531 | IMPIX-ALIF D 10mm at 6° |