Primary Device ID | 08800049286586 |
NIH Device Record Key | d31e288f-061c-4b9b-83f8-77f53354f122 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cylinder Screw |
Version Model Number | MSC 1604 |
Catalog Number | MSC 1604 |
Company DUNS | 631085206 |
Company Name | DIO Corporation |
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 | true |
Lot Batch | true |
Serial Number | true |
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 | 08800049286586 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800049286586]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-18 |
Device Publish Date | 2020-03-10 |
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08800049302330 - DIO Ratchet Wrench | 2023-09-18 |
08800049304129 - DIO Square Wrench | 2023-09-18 |
08800049306109 - DIO Torque Wrench | 2023-09-18 |
08800049251409 - UF(II) Scan Adapter | 2023-09-11 |
08800049430569 - UF(II) Eco Base Abutment | 2023-09-11 |
08800049430576 - UF(II) Eco Base Abutment | 2023-09-11 |
08800049430583 - UF(II) Eco Base Abutment | 2023-09-11 |