Primary Device ID | 04045396195493 |
NIH Device Record Key | 6d9d0b4e-f6f5-49dc-9816-f6e90d9facb2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Stethoscope duplex® 2.0 baby, red, |
Version Model Number | 4220-04 |
Catalog Number | 4220-04 |
Company DUNS | 537208717 |
Company Name | Rudolf Riester 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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04045396195493 [Primary] |
LDE | Stethoscope, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-02-05 |
Device Publish Date | 2021-01-28 |
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