| Primary Device ID | 08809702401199 | 
| NIH Device Record Key | aa72aae2-b245-4bca-8148-28e029635d37 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | KJ Mini Implant System | 
| Version Model Number | OBM5016 | 
| Company DUNS | 688476027 | 
| Company Name | KJMEDITECH.CO.,LTD | 
| 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 | true | 
| Expiration Date | true | 
| 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 | 08809702401199 [Primary] | 
| DZE | Implant, Endosseous, Root-Form | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2019-11-27 | 
| Device Publish Date | 2019-11-19 | 
| 08809702404534 | KJ Mini Implant System/Post Abutment | 
| 08809702404527 | KJ Mini Implant System/Post Abutment | 
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| 08809702404404 | KJ Mini Implant System/Post Abutment | 
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| 08809702404305 | KJ Mini Implant System/Post Abutment | 
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