Primary Device ID | 24053613279165 |
NIH Device Record Key | a7d670ef-b4fd-4c51-afaf-95e1a3983312 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PIN DRIVER |
Version Model Number | 02-029-99-1101 |
Catalog Number | 02-029-99-1101 |
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 | 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 | 04053613279161 [Direct Marking] |
GS1 | 14053613279168 [Primary] |
GS1 | 24053613279165 [Package] Contains: 14053613279168 Package: tubular bag [1 Units] In Commercial Distribution |
HIBCC | E226051714Q41 [Secondary] |
GFC | Driver, Surgical, Pin |
Steralize Prior To Use | true |
Device Is Sterile | false |
[24053613279165]
Moist Heat or Steam Sterilization
[24053613279165]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2020-04-03 |
Device Publish Date | 2018-12-21 |
24053613279165 | 02-029-99-1101 |
04053613283793 | GS900S.62.12.Q5 |
04053613282598 | GS900.55.11.Q5 |
04053613279673 | GS900.53.10.TW |
04053613279659 | GS900.55.20.Q5 |
04053613284349 | GS900.130.000.Q5 |
04053613284400 | GS900.100.000.Q5 |
04053613286107 | GS900.054.010,.K0 |