Primary Device ID | 04260223146138 |
NIH Device Record Key | 3886c452-ee25-427b-8898-3a86a4cc1b70 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Accessory Box AB08 |
Version Model Number | 100734-P |
Company DUNS | 551540334 |
Company Name | PATH medical GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | false |
Serial Number | false |
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 | 04260223146138 [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 | 2022-01-25 |
Device Publish Date | 2022-01-17 |
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