| Primary Device ID | 28800055100313 |
| NIH Device Record Key | 68b7e54d-c1e8-4728-b050-97336573a3a4 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MF SAFECATH |
| Version Model Number | SC107 |
| Catalog Number | Intravascular catheter 18Gx1.25" |
| Company DUNS | 688303694 |
| Company Name | Medifirst co., ltd. |
| Device Count | 50 |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 08800055100319 [Unit of Use] |
| GS1 | 18800055100316 [Primary] |
| GS1 | 28800055100313 [Package] Contains: 18800055100316 Package: Case [200 Units] In Commercial Distribution |
| FOZ | Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2020-08-18 |
| Device Publish Date | 2020-08-10 |
| 28800055100467 | SC110 |
| 28800055100450 | SS201 |
| 28800055100443 | SS202 |
| 28800055100436 | SS203 |
| 28800055100429 | SS204 |
| 28800055100412 | SS205 |
| 28800055100405 | SS206 |
| 28800055100399 | SS207 |
| 28800055100382 | SS208 |
| 28800055100375 | SC101 |
| 28800055100368 | SC102 |
| 28800055100351 | SC103 |
| 28800055100344 | SC104 |
| 28800055100337 | SC105 |
| 28800055100320 | SC106 |
| 28800055100313 | SC107 |
| 28800055100306 | SC108 |
| 28800055100290 | SC109 |