Primary Device ID | D962GGS00002 |
NIH Device Record Key | c8032d1b-6ae0-498c-b5a5-9421c0c0ccc9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Grin Scope |
Version Model Number | 3D Print Version |
Company DUNS | 117178760 |
Company Name | Get-Grin Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 |
---|---|
HIBCC | D962GGS00002 [Primary] |
DZN | Instruments, Dental Hand |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-20 |
Device Publish Date | 2020-08-12 |
D962GGS00002 | 3D Print Version |
D962GGS00001 | IM Version |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() GRIN SCOPE 90221213 not registered Live/Pending |
Get-Grin Inc. 2020-09-29 |