Primary Device ID | 08809917605931 |
NIH Device Record Key | f57af7cf-c51c-4224-a763-ac6a8b2a5945 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Scan Healing Abutment Screw |
Version Model Number | HAS-S17M |
Company DUNS | 557821945 |
Company Name | ARUM DENTISTRY Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 08809917605931 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-06-13 |
Device Publish Date | 2024-06-05 |
08800055793320 | HAS-S18R |
08800055793313 | HAS-S16R |
08800055793306 | HAS-S14R |
08800055793290 | HAS-S12R |
08800055793283 | HAS-S10R |
08809917605993 | HAS-S18R |
08809917605986 | HAS-S16R |
08809917605979 | HAS-S14R |
08809917605962 | HAS-S12R |
08809917605955 | HAS-S10R |
08809917605948 | HAS-S19M |
08809917605931 | HAS-S17M |
08809917605924 | HAS-S15M |
08809917605917 | HAS-S13M |
08809917605900 | HAS-S11M |