Primary Device ID | 00821925019065 |
NIH Device Record Key | 6f01c10a-5adc-4f34-9628-fd8a074a9f30 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SHAH VENT TUBE WO WIRE 114 MM ID FLUOROPLASTIC |
Version Model Number | 146044 |
Company DUNS | 007198742 |
Company Name | Gyrus Acmi, Inc. |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
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Device Issuing Agency | Device ID |
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GS1 | 00821925019065 [Package] Contains: 00821925034068 Package: [6 Units] In Commercial Distribution |
GS1 | 00821925034068 [Primary] |
ETD | Tube, Tympanostomy |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-10-24 |