Primary Device ID | M689HHCTUINK0105030 |
NIH Device Record Key | 4c00f56c-a8f2-4e81-a317-2c8fb97e38f4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Chest Tube Insertion Kit Cast of 5 |
Version Model Number | 03 |
Catalog Number | HHCTUINK01-05 |
Company DUNS | 118492643 |
Company Name | Safeguard US Operating, LLC |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | M689HHCTUINK0105030 [Primary] |
PYI | Thoracic Catheter Insertion Tray |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-07-01 |
Device Publish Date | 2025-06-23 |
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