Primary Device ID | 07613365000771 |
NIH Device Record Key | e879f789-c2cd-4055-93cb-6fe9f63a1c1d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Schiller NIBP connecting hose |
Version Model Number | 2.100795 |
Catalog Number | 2.100795 |
Company DUNS | 480868538 |
Company Name | Schiller AG |
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 | true |
Serial Number | false |
Manufacturing Date | false |
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 |
Phone | +41417664242 |
info@schiller.ch |
Storage Environment Temperature | Between -10 Degrees Celsius and 50 Degrees Celsius |
Storage Environment Temperature | Between -10 Degrees Celsius and 50 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07613365000771 [Primary] |
DXQ | Blood Pressure Cuff |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-10 |
Device Publish Date | 2016-09-20 |
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