Primary Device ID | 24053613292416 |
NIH Device Record Key | aad926ae-57e2-459f-ae99-3154b243af72 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bur, Round |
Version Model Number | 899722404 |
Catalog Number | 899722404 |
Company DUNS | 317409001 |
Company Name | Gebr. Brasseler 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 | 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 | 14053613292419 [Primary] |
GS1 | 24053613292416 [Package] Contains: 14053613292419 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 | 2025-09-08 |
Device Publish Date | 2025-08-29 |
24053613292997 | 899720405 |
24053613292980 | 899720404 |
24053613292973 | 899721304 |
24053613292966 | 899720304 |
24053613292959 | 899722403 |
24053613292942 | 899721403 |
24053613292935 | 899720403 |
24053613292423 | 899722405 |
24053613292416 | 899722404 |
24053613292393 | 899721405 |
24053613292386 | 899721404 |
24053613292355 | 899722304 |