Primary Device ID | 00850019808025 |
NIH Device Record Key | bfd1afd2-a108-42b5-b88c-6b90190d167b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuVein |
Version Model Number | HF570 |
Company DUNS | 807920546 |
Company Name | Accuvein Inc. |
Device Count | 1 |
DM Exempt | true |
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 | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850019808025 [Primary] |
KZA | Device, Vein Location, Liquid Crystal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-03-22 |
Device Publish Date | 2021-03-12 |
00850019808032 | Hands-Free Wheeled Stand |
00850019808025 | Powered Hands-Free Wheeled Stand |
00850019808018 | Infrared Vein Visualization Device |
00850019808049 | Hands-Free Arm with clamp |
00850019808070 | Powered, Goose Neck Hands-Free Wheeled Stand |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCUVEIN 77284704 3565545 Live/Registered |
ACCUVEIN INC. 2007-09-20 |