Primary Device ID | 05030267044467 |
NIH Device Record Key | 8bd82d6f-d539-43e6-96c5-a57e5a804b73 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GUEDEL AIRWAY, SIZE 1, ISO 6.5 |
Version Model Number | 1111065 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | true |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
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 | 05030267044467 [Package] Contains: 05030267050611 Package: [20 Units] In Commercial Distribution |
GS1 | 05030267044474 [Package] Contains: 05030267050611 Package: [80 Units] In Commercial Distribution |
GS1 | 05030267050611 [Primary] |
CAE | Airway, Oropharyngeal, Anesthesiology |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-02 |
Device Publish Date | 2023-05-25 |
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