| Primary Device ID | 10709078005289 |
| NIH Device Record Key | 439c4ead-73f8-4f3a-ac2a-fac028eaafb3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Uni-lim Coaxial Circuit |
| Version Model Number | 9626 |
| Company DUNS | 092673953 |
| Company Name | WESTMED, INC. |
| 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 | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| 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 | 00709078005282 [Primary] |
| GS1 | 10709078005289 [Package] Contains: 00709078005282 Package: [20 Units] In Commercial Distribution |
| OFP | Anesthesia Breathing Circuit Kit (Adult & Pediatric) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-11-27 |
| Device Publish Date | 2018-02-05 |
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