Primary Device ID | 00670082000511 |
NIH Device Record Key | 4a5a2d33-7218-44ca-b672-bf1a39ad5ca6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Modus Plan |
Version Model Number | 2.1 |
Catalog Number | SYN-0866 |
Company DUNS | 203061833 |
Company Name | Synaptive Medical 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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00670082000511 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2023-10-18 |
Device Publish Date | 2022-12-13 |
00670082000443 | 2.0 |
00670082000511 | 2.1 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MODUS PLAN 87597878 not registered Live/Pending |
SYNAPTIVE MEDICAL (BARBADOS) INC. 2017-09-06 |