Primary Device ID | 00872320003449 |
NIH Device Record Key | e742f619-9bcf-427b-9964-6f27123c80e9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Precise LTM 60° Tip |
Version Model Number | 00669 |
Company DUNS | 102422578 |
Company Name | CAO GROUP, 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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00872320003135 [Package] Package: Pack [20 Units] In Commercial Distribution |
GS1 | 00872320003449 [Primary] |
GS1 | 00872320004415 [Package] Package: Pack [20 Units] In Commercial Distribution |
GEX | Powered Laser Surgical Instrument |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2018-11-08 |
Device Publish Date | 2016-11-10 |
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