Primary Device ID | 08800039376235 |
NIH Device Record Key | cceca20e-dcef-4528-81c1-cbdbea6b8883 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Magic Tap Guide |
Version Model Number | MPS |
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 Safe |
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 | 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 | 08800039376235 [Primary] |
DZA | Drill, Dental, Intraoral |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800039376235]
Moist Heat or Steam Sterilization
[08800039376235]
Moist Heat or Steam Sterilization
[08800039376235]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-09-01 |
Device Publish Date | 2022-04-11 |
08800039376259 | MPL |
08800039376242 | MPM |
08800039376235 | MPS |