Primary Device ID | 00850007069704 |
NIH Device Record Key | df785985-34e0-446e-84c2-b4777cb0b6b3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MISScope 4K |
Version Model Number | VSY-2250 |
Company DUNS | 096680671 |
Company Name | VISEON, 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 | true |
Expiration Date | true |
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 | 00850007069704 [Primary] |
HRX | Arthroscope |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-02-13 |
Device Publish Date | 2024-02-05 |
00850007069735 | MISScope 4K, 22 Dia, 80L |
00850007069728 | MISScope 4K, 22 Dia, 70L |
00850007069711 | MISScope 4K, 22 Dia, 60L |
00850007069704 | MISScope 4K, 22 Dia, 50L |
00850007069698 | MISScope 4K, 22 Dia, 40L |
00850007069681 | MISScope 4K, 18 Dia, 80L |
00850007069674 | MISScope 4K, 18 Dia, 70L |
00850007069667 | MISScope 4K, 18 Dia, 60L |
00850007069643 | MISScope 4K, 18 Dia, 40L |
00850007069650 | MISScope 4K, 18 Dia, 50L |