Primary Device ID | 00612649212722 |
NIH Device Record Key | c6150ec4-7e39-47e3-bc9e-5cc1bffefe77 |
Commercial Distribution Discontinuation | 2023-08-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | KING LTS-D Kit |
Version Model Number | KLTSD432 |
Catalog Number | KLTSD432 |
Company DUNS | 009299017 |
Company Name | King Systems Corporation |
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 | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com | |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00612649212722 [Package] Contains: 00612649212739 Package: [5 Units] Discontinued: 2023-08-31 Not in Commercial Distribution |
GS1 | 00612649212739 [Primary] |
CAE | AIRWAY, OROPHARYNGEAL, ANESTHESIOLOGY |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-10-25 |
Device Publish Date | 2022-12-08 |
00612649212753 | AMBU / KING LTSD, SIZE 2.5,W/SUCTION PORT, NON-STERILE KIT |
00612649212722 | AMBU / KING LTSD, SIZE 2,W/SUCTION PORT, NON-STERILE KIT |
00612649212715 | AMBU / KING LTSD, SIZE 1,W/SUCTION PORT, NON-STERILE KIT |
00612649212692 | AMBU / KING LTSD, SIZE 0,W/SUCTION PORT, NON-STERILE KIT |