Primary Device ID | 08436031030716 |
NIH Device Record Key | 4cd015d3-b1af-4dd9-9f2d-5e10f8cd799e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Airtraq |
Version Model Number | A-071 |
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 | 08436031030716 [Primary] |
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 |
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48436031030516 | Airtraq SP Infant Nasal |
48436031030417 | Airtraq SP Infant |
48436031030318 | Airtraq SP Pediatric |
48436031030219 | Airtraq SP Small |
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