Primary Device ID | 04546540366795 |
NIH Device Record Key | 396ba82e-d0bc-454b-a0e7-dedc476cb953 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 62-20523 |
Catalog Number | 62-20523 |
Company DUNS | 316153956 |
Company Name | Stryker Leibinger GmbH & Co. KG |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
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 | false |
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 |
Length | 30 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540366795 [Primary] |
HTW | BIT, DRILL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04546540366795]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2016-10-19 |
07613327616118 - N/A | 2024-08-30 Spine Guidance 5 Software |
07613327616255 - N/A | 2024-08-23 Spine Guidance 5 Enable |
07613327616286 - N/A | 2024-08-23 Spine Guidance 5 Sales Demo |
07613327638189 - N/A | 2024-08-23 Spine Guidance 5 Upgrade |
07613327638196 - N/A | 2024-08-23 Spine Guidance 5 Update |
07613327579833 - N/A | 2024-08-15 Tracker-70 |
07613327579888 - N/A | 2024-08-15 Tracking Instrument Battery |
07613327635102 - NA | 2024-07-18 Neuro Dynamic Mesh L |