Primary Device ID | 30866479000115 |
NIH Device Record Key | 0d83323d-a9c4-4373-957f-f9317f828f1a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BEACON |
Version Model Number | BM1412-50-F-1 |
Company DUNS | 078473721 |
Company Name | SCION MEDICAL TECHOLOGIES, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00866479000114 [Primary] |
GS1 | 30866479000115 [Package] Contains: 00866479000114 Package: [10 Units] In Commercial Distribution |
NEU | Marker, Radiographic, Implantable |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-30 |
30866479000115 | Beacon Tissue Marker/Beacon Tissue Marker (SE) is a sterile, single patient use, PEKK discrete m |
00866479000107 | Beacon Tissue Marker/Beacon Tissue Marker (SE) is a sterile, single patient use, PEKK discrete m |