Primary Device ID | 00850075255030 |
NIH Device Record Key | 1be4b0a7-39f0-47b3-b08d-58414a3c9ad4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Med-Tech Resource |
Version Model Number | CP6331 |
Company DUNS | 929948917 |
Company Name | Med-Tech Resource, LLC |
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 | true |
Donation Id Number | true |
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 | 00850075255030 [Primary] |
BTM | Ventilator, Emergency, Manual (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-10 |
Device Publish Date | 2025-06-02 |
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