Primary Device ID | 04260223143335 |
NIH Device Record Key | a6340d9a-a04d-4a17-a587-f9d6940666f2 |
Commercial Distribution Discontinuation | 2020-06-29 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Sentiero Basic AuDX Set |
Version Model Number | 100250-BL1 |
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 | 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 | 04260223143335 [Primary] |
GWJ | Stimulator, Auditory, Evoked Response |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-06-30 |
Device Publish Date | 2018-04-10 |
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