Primary Device ID | 05030267011674 |
NIH Device Record Key | b322b591-d8c7-4cfc-b781-22e4ed6cd692 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MONITORING LINE 1.8M, MALE - MALE LUER LOCK CONNECTORS |
Version Model Number | 2725000 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | true |
Single Use | false |
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 | 05030267011674 [Package] Contains: 05030267064823 Package: [20 Units] In Commercial Distribution |
GS1 | 05030267011681 [Package] Contains: 05030267064823 Package: [80 Units] In Commercial Distribution |
GS1 | 05030267064823 [Primary] |
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 | 2024-02-28 |
Device Publish Date | 2024-02-20 |
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