Primary Device ID | D1057118L1000 |
NIH Device Record Key | c5f2fd9c-4cfc-4ed8-868d-25c23b8ee8ea |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SurgiMac |
Version Model Number | 7119-XL-Case |
Company DUNS | 060635048 |
Company Name | Surgimac LLC |
Device Count | 1000 |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D1057118L1000 [Unit of Use] |
HIBCC | DSCASE7118 [Primary] |
HIBCC | DSCASE7119 [Primary] |
LYY | Latex 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 | 2023-10-17 |
Device Publish Date | 2023-10-09 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SURGIMAC 90034986 not registered Live/Pending |
Waseem, Umair 2020-07-03 |