Primary Device ID | 03664188000107 |
NIH Device Record Key | 1a693d80-a788-4874-85e5-8ea9a91822b4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Luneau |
Version Model Number | Tonometer separation prisms L900 -box of 100 |
Company DUNS | 260432380 |
Company Name | LUNEAU TECHNOLOGY OPERATIONS |
Device Count | 100 |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03664188000107 [Primary] |
GS1 | 03664188000114 [Unit of Use] |
HKY | Tonometer, Manual |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-05-15 |
Device Publish Date | 2016-09-23 |
03664188000107 | The separation prisms is an accessory to the tonometer which is device intended to estimate intr |
03664188000114 | The separation prisms is an accessory to the tonometer which is device intended to estimate intr |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
LUNEAU 74696483 2036550 Dead/Cancelled |
LUNEAU, S.A. 1995-06-21 |
LUNEAU 74380876 1900512 Dead/Cancelled |
LUNEAU S.A. 1993-04-16 |
LUNEAU 73236874 1186076 Dead/Cancelled |
Luneau U.S.A., Inc. 1979-10-29 |
LUNEAU 73236353 1175624 Dead/Cancelled |
Luneau U.S.A., Inc. 1979-10-23 |