Primary Device ID | D1052219XL1000 |
NIH Device Record Key | 685a722a-4ed7-4dfd-b127-73a7c8f0ede1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SurgiMac |
Version Model Number | 2219XL-Case |
Company DUNS | 060635048 |
Company Name | Surgimac LLC |
Device Count | 2000 |
DM Exempt | false |
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 | false |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D1052219XL1000 [Unit of Use] |
HIBCC | DXLCASE2219 [Primary] |
LZA | Polymer Patient Examination Glove |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-27 |
Device Publish Date | 2023-06-19 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SURGIMAC 90034986 not registered Live/Pending |
Waseem, Umair 2020-07-03 |