Primary Device ID | 04546540366702 |
NIH Device Record Key | 766c81dc-bec8-4d94-8556-bdceeb2b36c5 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 62-17517 |
Catalog Number | 62-17517 |
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 | 04546540366702 [Primary] |
HTW | BIT, DRILL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04546540366702]
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 |
07613327556285 - NA | 2024-02-27 Facial iD MF 1 Mesh |
07613327556308 - NA | 2024-02-23 Facial iD MF 2 meshes |
07613327556322 - NA | 2024-02-23 Facial iD MF 3 meshes |
07613327556346 - NA | 2024-02-23 Facial iD MF 4 meshes |
07613327556377 - NA | 2024-02-23 Facial iD MF 5 meshes |
07613327556391 - NA | 2024-02-23 Facial iD MF 6 meshes |
07613327556827 - NA | 2024-02-23 Facial iD MF 1 mesh kit |
07613327556834 - NA | 2024-02-23 Facial iD MF 3 meshes kit |