| 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 |
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 |