Primary Device ID | 08800039301220 |
NIH Device Record Key | 1614371c-2ca0-489e-b307-6249203a5ab2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical Guide Sinus Lifter |
Version Model Number | FSMSL |
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 | 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 | 08800039301220 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800039301220]
Moist Heat or Steam Sterilization
[08800039301220]
Moist Heat or Steam Sterilization
[08800039301220]
Moist Heat or Steam Sterilization
[08800039301220]
Moist Heat or Steam Sterilization
[08800039301220]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-26 |
Device Publish Date | 2022-05-18 |
08800039301237 | MSMSL |
08800039301220 | FSMSL |