Primary Device ID | 20889483230401 |
NIH Device Record Key | 598e4345-e93d-4ccb-a66c-b4dd97a81e2b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Gas Sampling Lines |
Version Model Number | 0940 |
Company DUNS | 022721133 |
Company Name | SALTER LABS |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
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 | 10889483230404 [Primary] |
GS1 | 20889483230401 [Package] Contains: 10889483230404 Package: [25 Units] In Commercial Distribution |
CCK | Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-11-08 |
Device Publish Date | 2023-10-31 |
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