Primary Device ID | 00817495023311 |
NIH Device Record Key | dcd11778-0309-43ca-b5af-18c60740cb90 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Matrix Pro |
Version Model Number | AS09627 |
Company DUNS | 053468385 |
Company Name | CANDELA CORPORATION |
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 | 00817495023311 [Primary] |
GS1 | 47290109952961 [Previous] |
GEI | Electrosurgical, Cutting & Coagulation & Accessories |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-30 |
Device Publish Date | 2022-05-20 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MATRIX PRO 97024406 not registered Live/Pending |
Candela Corporation 2021-09-13 |
![]() MATRIX PRO 90677928 not registered Live/Pending |
Freedom Pro Wrestling,LLC 2021-04-28 |
![]() MATRIX PRO 87902538 not registered Live/Pending |
Matrix Holding Group LLC 2018-05-01 |
![]() MATRIX PRO 76497451 not registered Dead/Abandoned |
Folsom Research, Inc. 2003-03-14 |