Primary Device ID | 04589551354931 |
NIH Device Record Key | 0cc8a870-f55a-4cc3-a80f-3f735155c0c4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PD-CTAD-G |
Version Model Number | PD-CTAD-G |
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 | true |
Serial Number | false |
Manufacturing Date | false |
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 | 04589551354900 [Primary] |
GS1 | 04589551354931 [Direct Marking] |
HWE | INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-18 |
Device Publish Date | 2022-05-10 |
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04589551389391 - Surgic Pro2 OPT | 2024-10-23 |