Primary Device ID | 07640187463378 |
NIH Device Record Key | 73bf4f63-8ccc-4404-a9c8-0e5861e8f707 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SALTI Anterolateral Template |
Version Model Number | B-420042 |
Company DUNS | 480244832 |
Company Name | Bonebridge AG |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07640187463378 [Primary] |
HWT | Template |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
[07640187463378]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-31 |
Device Publish Date | 2025-07-23 |