Primary Device ID | 00852205007991 |
NIH Device Record Key | 870e443a-d893-496a-8e3c-257e31dc52b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medrobotics |
Version Model Number | 23024 |
Catalog Number | 23024 |
Company DUNS | 014464314 |
Company Name | EXACT MEDICAL MANUFACTURING, INC. |
Device Count | 1 |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00852205007984 [Primary] |
GS1 | 00852205007991 [Package] Contains: 00852205007984 Package: Case [10 Units] In Commercial Distribution |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-11-26 |
Device Publish Date | 2018-10-24 |
00852205007991 | Flex Monitor Cover |
10850003355006 | Flex Console Cover |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() MEDROBOTICS 85366415 4432944 Live/Registered |
MEDROBOTICS CORPORATION 2011-07-08 |
![]() MEDROBOTICS 85347815 4344315 Live/Registered |
MEDROBOTICS CORPORATION 2011-06-16 |