Primary Device ID | 10848340009638 |
NIH Device Record Key | 7c2a742a-14d2-41b7-bf19-5a537981d838 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Snap Kover |
Version Model Number | 02-5490TL |
Company DUNS | 130785884 |
Company Name | ADVANCE MEDICAL DESIGNS, INC. |
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 | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00848340009631 [Primary] |
GS1 | 10848340009638 [Package] Contains: 00848340009631 Package: [50 Units] In Commercial Distribution |
JAA | System, x-ray, fluoroscopic, image-intensified |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-23 |
Device Publish Date | 2022-06-15 |
10848340015424 | Disposable Equipment Cover |
10848340009638 | Disposable Equipment Cover |
10848340018975 | Non-Sterile |
10848340018753 | Non-Sterile |
10848340019781 | Disposable Equipment Cover |
10848340016865 | Snap Kover |
10848340017022 | Snap Kover |
10848340009621 | Snap Kover |
10848340002318 | w/Additional Band |