Primary Device ID | 00817493026369 |
NIH Device Record Key | 58bc7827-cb71-4cd8-b0ba-c049cf3bfb5f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hive TL Interbody System |
Version Model Number | 05-A-0001-4010 |
Catalog Number | 05-A-0001-4010 |
Company DUNS | 080469093 |
Company Name | Nanohive Medical LLC |
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 | true |
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 |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Width | 11 Millimeter |
Length | 32 Millimeter |
Height | 10 Millimeter |
Angle | 8 degree |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817493026369 [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 | 2023-09-18 |
Device Publish Date | 2023-09-08 |
00817493026413 | 11W x 32L x 15H, 8° - Tube Package Configuration |
00817493026406 | 11W x 32L x 14H, 8° - Tube Package Configuration |
00817493026390 | 11W x 32L x 13H, 8° - Tube Package Configuration |
00817493026383 | 11W x 32L x 12H, 8° - Tube Package Configuration |
00817493026376 | 11W x 32L x 11H, 8° - Tube Package Configuration |
00817493026369 | 11W x 32L x 10H, 8° - Tube Package Configuration |
00817493026352 | 11W x 32L x 9H, 8° - Tube Package Configuration |
00817493026345 | 11W x 32L x 8H, 8° - Tube Package Configuration |
00817493026338 | 11W x 32L x 7H, 8° - Tube Package Configuration |