Primary Device ID | 10816058012196 |
NIH Device Record Key | 4deb9448-81c6-4042-a94f-9f8401808535 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Hyundai |
Version Model Number | K2F72AU100 XX |
Catalog Number | K2F72AU100 XX |
Company DUNS | 196527949 |
Company Name | DC Safety Sales |
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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00816058012199 [Primary] |
GS1 | 10816058012196 [Package] Contains: 00816058012199 Package: Bag [1 Units] In Commercial Distribution |
GS1 | 30816058012190 [Package] Package: Case (bagged) [3 Units] In Commercial Distribution |
LRR | First Aid Kit With Drug |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-07-24 |
Device Publish Date | 2023-07-14 |
00816058012847 | First Aid Kit |
10816058012134 | Roadside Assistance Kit |
10816058012196 | Severe Weather Kit |
10816058012400 | PPE Kit |