| Primary Device ID | 20840682102814 |
| NIH Device Record Key | d2f96782-bd38-41e8-90da-1d2414db2ab2 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | D-fend Water Trap, 881319-HEL |
| Company DUNS | 401966697 |
| Company Name | GE Healthcare Finland Oy |
| 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 | true |
| Lot Batch | true |
| 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 | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00840682102810 [Primary] |
| GS1 | 20840682102814 [Package] Contains: 00840682102810 Package: [10 Units] In Commercial Distribution |
| NHO | Analyzer, gas, desflurane, gaseous-phase (anesthetic concentration) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-08-15 |
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