| Primary Device ID | 05030267167166 | 
| NIH Device Record Key | 946103b4-5ef1-447d-9a94-228c7a041562 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | CLEARLITE™ AIR, ANAESTHETIC FACE MASK SIZE 4 ADULT GREEN SEAL NO HOOK RING 22F | 
| Version Model Number | 7394001 | 
| 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 | 05030267167159 [Primary] | 
| GS1 | 05030267167166 [Package] Contains: 05030267167159 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  |