Primary Device ID | 08806195983737 |
NIH Device Record Key | 990f0c4f-7b08-40a3-9fdc-2266a8b1c557 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | UF(II) Fixture |
Version Model Number | UF(II) 4005UV3 |
Catalog Number | UF(II) 4005UV3 |
Company DUNS | 631085206 |
Company Name | DIO Corporation |
Device Count | 1 |
DM Exempt | true |
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 | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08806195983737 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-04-07 |
Device Publish Date | 2022-03-30 |
08806195983799 | UF(II) 6505UV3 |
08806195983782 | UF(II) 6005UV3 |
08806195983775 | UF(II) 5505UV3 |
08806195983768 | UF(II) 5005UV3 |
08806195983751 | UF(II) 4505UV3 |
08806195983744 | UF(II) 4007UV3 |
08806195983737 | UF(II) 4005UV3 |
08806195983720 | UF(II) 7005SF |
08806195983713 | UF(II) 6505SF |
08806195983706 | UF(II) 6005SF |
08806195983690 | UF(II) 5505SF |
08806195983683 | UF(II) 5005SF |
08806195983676 | UF(II) 4505SF |
08806195983669 | UF(II) 4007SF |
08806195983652 | UF(II) 4005SF |
08806195983645 | UF(II) 7005S |
08806195983638 | UF(II) 6505S |
08806195983621 | UF(II) 6005S |
08806195983614 | UF(II) 5505S |
08806195983607 | UF(II) 5005S |
08806195983591 | UF(II) 4505S |
08806195983584 | UF(II) 4007S |
08806195983577 | UF(II) 4005S |