| Primary Device ID | 04048675398639 |
| NIH Device Record Key | 28e9ee74-b478-4dfa-9ee7-6bd15aa7d6a6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ponta Shuttle E/S plus |
| Version Model Number | G16703 |
| Company DUNS | 315578914 |
| Company Name | Drägerwerk AG & Co. KGaA |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 04048675398639 [Primary] |
| FQO | Table, Operating-Room, Ac-Powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-07-06 |
| Device Publish Date | 2022-06-28 |
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