Primary Device ID | 24053613288433 |
NIH Device Record Key | 3cb82f3d-db2a-40d3-a5d2-7e58f4fda54b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Brophy |
Version Model Number | DB501570R-S |
Catalog Number | DB501570R-S |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler 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 | true |
Expiration Date | true |
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 | 14053613288436 [Primary] |
GS1 | 24053613288433 [Package] Contains: 14053613288436 Package: [5 Units] In Commercial Distribution |
GFF | Bur, Surgical, General & Plastic Surgery |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-03-07 |
Device Publish Date | 2024-02-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BROPHY 98200475 not registered Live/Pending |
Brophy College Preparatory 2023-09-27 |
BROPHY 86171307 4824772 Live/Registered |
Brophy Engraving Company 2014-01-21 |