Primary Device ID | 04589551392889 |
NIH Device Record Key | 4074b2a3-5086-4d40-b77b-b8b383cc07e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgic Pro2 NON-OPT |
Version Model Number | Surgic Pro2 NON-OPT |
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 | 04589551392889 [Primary] |
EBW | Controller, foot, handpiece and cord |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
[04589551392889]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-09-03 |
Device Publish Date | 2025-08-26 |
04589551389407 | Surgic Pro2 NON-OPT |
04589551392889 | Surgic Pro2 NON-OPT |