Primary Device ID | 06923980101939 |
NIH Device Record Key | 67203a00-8c4b-4e07-b082-c99a27f3d008 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | AW0006 |
Catalog Number | AW0006 |
Company DUNS | 527333326 |
Company Name | GaleMed Xiamen Co., Ltd. |
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 | 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 | 06923980101939 [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 | 2023-08-24 |
Device Publish Date | 2023-08-16 |
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