Primary Device ID | 10848340009881 |
NIH Device Record Key | f663e403-65f0-423b-ab82-fdb47636f5e8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micro Kover |
Version Model Number | MK974NS |
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 | 00848340009884 [Primary] |
GS1 | 10848340009881 [Package] Contains: 00848340009884 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 | 2022-12-06 |
Device Publish Date | 2022-11-28 |
10848340009881 | Disposable Equipment Cover |
10848340020145 | Micro Kover |
10848340020183 | Micro Kover |
10848340020176 | Micro Kover |
10848340020169 | Micro Kover |
10848340009935 | Micro Kover |
10848340020213 | Micro Kover |
10848340009959 | Micro Kover |
10848340009942 | Micro Kover |
10848340020220 | Micro Kover |
10848340009966 | Micro Kover |