Primary Device ID | 08809986606945 |
NIH Device Record Key | f6898aea-7d9a-47f2-8d56-06769ee833da |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Magic Depth Drill |
Version Model Number | MDDA |
Company DUNS | 631169224 |
Company Name | InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd) |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
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 | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | true |
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 | 08809986606945 [Primary] |
DZA | Drill, Dental, Intraoral |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08809986606945]
Moist Heat or Steam Sterilization
[08809986606945]
Moist Heat or Steam Sterilization
[08809986606945]
Moist Heat or Steam Sterilization
[08809986606945]
Moist Heat or Steam Sterilization
[08809986606945]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-23 |
Device Publish Date | 2024-12-13 |
08809986606945 - Magic Depth Drill | 2024-12-23 |
08809986606945 - Magic Depth Drill | 2024-12-23 |
08800039335393 - Magicore S | 2024-12-05 |
08800039335409 - Magicore S | 2024-12-05 |
08800039335416 - Magicore S | 2024-12-05 |
08800039335423 - Magicore S | 2024-12-05 |
08800039336697 - Magicore S | 2024-12-05 |
08800039336703 - Magicore S | 2024-12-05 |
08800039336710 - Magicore S | 2024-12-05 |