Primary Device ID | M68920510030 |
NIH Device Record Key | 824d1735-2e59-4fe5-be16-bbbcbf13b53b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sentinel Chest Trauma Kit |
Version Model Number | 03 |
Catalog Number | 20-510 |
Company DUNS | 118492643 |
Company Name | Safeguard US Operating, LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
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 | M68920510030 [Primary] |
GAA | Needle, Aspiration And Injection, Disposable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-04-12 |
Device Publish Date | 2018-09-13 |
M68920510030 | SENTINEL CHEST TRAUMA KIT 2 ea Sentinel Dual vent Chest seals with Sentinel 10x extreme strength |
M68920510050 | SENTINEL CHEST TRAUMA KIT 2 ea - Sentinel Dual vent Chest seals with Sentinel 10x extreme streng |
M68920510060 | SENTINEL CHEST TRAUMA KIT 2 ea - Sentinel Dual vent Chest seals with Sentinel 10x extreme streng |
M68920510070 | SENTINEL CHEST TRAUMA KIT 2 ea - Sentinel Dual vent Chest seals with Sentinel 10x extreme streng |