Primary Device ID | 00840199500321 |
NIH Device Record Key | 0f4d3170-1982-4fca-a0bb-d1e00416eeaf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cervical Graft Driver |
Version Model Number | 7222-35 |
Catalog Number | 7222-35 |
Company DUNS | 007928633 |
Company Name | KOROS U.S.A., INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
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 |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com | |
Phone | 1-805-529-0825 |
customerservice@korosUSA.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Special Storage Condition, Specify | Between 0 and 0 *Store in dry place at room temperature |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840199500321 [Direct Marking] |
GS1 | 10840199500328 [Primary] |
KWP | Appliance, Fixation, Spinal Interlaminal |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
[00840199500321]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-01 |
Device Publish Date | 2022-06-23 |
10840199500359 | Cervical Graft Driver Unguarded |
10840199500342 | Cervical Graft Driver Guarded |
00840199500321 | Cervical Graft Driver Guarded 7x12mm |
00840199500338 | Cervical Graft Driver Unguarded 7x12mm |