| Primary Device ID | 00850038863067 | 
| NIH Device Record Key | 47b677fc-e2d2-4570-8dc7-dad98641e170 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Fresnius Kabi AG | 
| Version Model Number | FK50060S | 
| Company DUNS | 969484237 | 
| Company Name | Directmed, Inc. | 
| 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 | true | 
| RX Perscription | true | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 00850038863067 [Primary] | 
| FPA | Set, Administration, Intravascular | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2023-11-08 | 
| Device Publish Date | 2023-10-31 | 
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| 10850038863057 | 30” Minibore Extension Set with slide clamp, male luer-lock and female luer | 
| 10850038863040 | 18" Standard bore Extension Set with 1.2 Micron Filter, pinch clamp, male luer-lock and female | 
| 10850038863033 | 18" Standard bore Extension Set with 0.2 Micron Filter, pinch clamp, male luer-lock and female | 
| 00850038863067 | 60” Minibore Extension Set with slide clamp, male luer-lock and female luer | 
| 00850038863050 | 30” Minibore Extension Set with slide clamp, male luer-lock and female luer | 
| 00850038863043 | 18" Standard bore Extension Set with 1.2 Micron Filter, pinch clamp, male luer-lock and female | 
| 00850038863036 | 18" Standard bore Extension Set with 0.2 Micron Filter, pinch clamp, male luer-lock and female |