Primary Device ID | 00382830062008 |
NIH Device Record Key | 7b956e0d-8230-4f82-9da5-88dd6bf46969 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ALGO Pro |
Version Model Number | 036234 |
Company DUNS | 245258280 |
Company Name | XLTEK |
Device Count | 1 |
DM Exempt | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00382830062008 [Primary] |
GWJ | Stimulator, Auditory, Evoked Response |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-04-03 |
Device Publish Date | 2024-03-26 |
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