Primary Device ID | 04560264559363 |
NIH Device Record Key | b65ed7be-861e-4dc3-8f50-87d7dbae4397 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | M900K |
Version Model Number | M900K |
Company DUNS | 690710546 |
Company Name | NAKANISHI INC. |
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 | false |
Lot Batch | false |
Serial Number | true |
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 | 04560264559363 [Direct Marking] |
GS1 | 04560264570412 [Primary] |
EFB | Handpiece, air-powered, dental |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
[04560264559363]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-11-02 |
Device Publish Date | 2022-10-25 |
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