| Primary Device ID | 18148440001009 | 
| NIH Device Record Key | 23439674-4491-4807-9868-cf5811a9c2f4 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Curlin | 
| Version Model Number | 1 | 
| Catalog Number | 360-2030 | 
| Company DUNS | 612746933 | 
| Company Name | ZEVEX INTERNATIONAL, INC. | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Unsafe | 
| Human Cell/Tissue Product | false | 
| Device Kit | false | 
| Device Combination Product | false | 
| Single Use | false | 
| Lot Batch | false | 
| Serial Number | false | 
| Manufacturing Date | false | 
| Expiration Date | false | 
| 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 | 18148440001009 [Primary] | 
| FRN | Pump, Infusion | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2018-09-03 | 
| Device Publish Date | 2018-08-03 | 
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