Primary Device ID | 04546540134561 |
NIH Device Record Key | 81d1d434-88a0-4c97-b2bd-3c7da73ddc2b |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 01-02960 |
Catalog Number | 01-02960 |
Company DUNS | 316153956 |
Company Name | Stryker Leibinger GmbH & Co. KG |
Device Count | 1 |
DM Exempt | false |
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 | true |
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 | 15 Centimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04546540134561 [Primary] |
EHO | BAR, PREFORMED |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04546540134561]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-10-19 |
07613327300024 - NA | 2024-04-18 |
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 |