Primary Device ID | 08800053007283 |
NIH Device Record Key | eae69c60-5603-4131-be7c-22cd8af8eed3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SQ Guide No-Mount Driver |
Version Model Number | DSQGNDRRL |
Company DUNS | 694721181 |
Company Name | DENTIS CO. ,LTD |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
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 | 08800053007283 [Primary] |
NDP | Accessories, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
[08800053007283]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-06-09 |
Device Publish Date | 2021-06-01 |
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