Primary Device ID | 07290114061193 |
NIH Device Record Key | 616d5728-d0a5-40d6-bb73-e4a9985d5d35 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Headstage Sterilization Net Tray |
Version Model Number | 1 |
Catalog Number | 366-000422-22 |
Company DUNS | 531856466 |
Company Name | ALPHA OMEGA ENGINEERING CO. LTD. |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290114061193 [Primary] |
GZL | Electrode, Depth |
Steralize Prior To Use | true |
Device Is Sterile | false |
[07290114061193]
Moist Heat or Steam Sterilization
[07290114061193]
Moist Heat or Steam Sterilization
[07290114061193]
Moist Heat or Steam Sterilization
[07290114061193]
Moist Heat or Steam Sterilization
[07290114061193]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-08 |
Device Publish Date | 2022-05-31 |
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