Primary Device ID | 08175700156059 |
NIH Device Record Key | f1a891a2-2ea7-48ad-aa6a-77e8afc681aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Scleral Depressors |
Version Model Number | AS14-110S-Med |
Catalog Number | AS14-110S-Med |
Company DUNS | 968368832 |
Company Name | AURORA SURGICAL, LLC |
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 | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08175700156059 [Primary] |
HNX | Depressor, Orbital |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
[08175700156059]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-13 |
Device Publish Date | 2023-12-05 |
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