Primary Device ID | 00821925039681 |
NIH Device Record Key | a5a0c925-2ab8-4fac-92ad-d19b9d4c266c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ARMSTRONG BEVELED GROMMET VENTILATION TUBES 114MM ID BLUE FLUOROPLASTIC |
Version Model Number | 70145761 |
Company DUNS | 007198742 |
Company Name | Gyrus Acmi, Inc. |
Device Count | 2 |
DM Exempt | false |
Pre-market Exempt | false |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
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Device Issuing Agency | Device ID |
---|---|
GS1 | 00821925024809 [Package] Package: [60 Units] In Commercial Distribution |
GS1 | 00821925039681 [Primary] |
GS1 | 00821925040816 [Unit of Use] |
ETD | Tube, Tympanostomy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-10-24 |
00821925039681 | Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear whi |
00821925021624 | Ventilate the middle ear subsequent to otitis media Elimiate fluid buildup in the middle ear whi |