Primary Device ID | 05030267167142 |
NIH Device Record Key | 0fcb3102-b865-489b-bc8b-4ababba303a8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CLEARLITE™ AIR, ANAESTHETIC FACE MASK, SIZE 4, ADULT, GREEN SEAL, 22F |
Version Model Number | 7394000 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05030267167135 [Primary] |
GS1 | 05030267167142 [Package] Contains: 05030267167135 Package: [35 Units] In Commercial Distribution |
BSJ | Mask, Gas, Anesthetic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-17 |
Device Publish Date | 2024-10-09 |
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Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CLEARLITE 79249720 5911173 Live/Registered |
Imerys Filtration France 2018-06-05 |
![]() CLEARLITE 78241049 2934085 Live/Registered |
OFS FITEL, LLC 2003-04-23 |
![]() CLEARLITE 75056335 2030174 Dead/Cancelled |
GEJEIAN, MIKE 1996-02-12 |
![]() CLEARLITE 74636242 1951162 Dead/Cancelled |
Double L Group, Ltd. 1995-02-21 |
![]() CLEARLITE 74389567 1828425 Dead/Cancelled |
Life Services Supplements, Inc. 1993-05-12 |