| Primary Device ID | 48436031030219 |
| NIH Device Record Key | 8931b365-ec38-4311-a92e-35458cc9961a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Airtraq |
| Version Model Number | A-021 |
| Company DUNS | 541001090 |
| Company Name | PRODOL MEDITEC, SA |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | MR Conditional |
| 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 | 08436031030211 [Primary] |
| GS1 | 38436031030212 [Package] Package: Box [30 Units] In Commercial Distribution |
| GS1 | 48436031030219 [Package] Contains: 08436031030211 Package: Box [2 Units] In Commercial Distribution |
| CCW | Laryngoscope, Rigid |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-08-09 |
| Device Publish Date | 2023-08-01 |
| 78436031035901 | Airtraq Avant Docking Station |
| 68436031035218 | Airtraq Avant Small Blade |
| 68436031035119 | Airtraq Avant Regular Blade |
| 78436031035017 | Airtraq Avant Optics |
| 78436031033921 | Airtraq A-390 WiFi Camera KIT |
| 78436031033907 | Airtraq A-390 WiFi Camera |
| 08436031030716 | Airtraq SP Double Lumen |
| 48436031030615 | Airtraq SP Adult Nasal |
| 48436031030516 | Airtraq SP Infant Nasal |
| 48436031030417 | Airtraq SP Infant |
| 48436031030318 | Airtraq SP Pediatric |
| 48436031030219 | Airtraq SP Small |
| 48436031030110 | Airtraq SP Regular |