Primary Device ID | 00850200006261 |
NIH Device Record Key | 26c073b8-2cf2-4502-9337-25e56d665b1f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | McCarus-Volker FORNISEE® System |
Version Model Number | 110029 |
Company DUNS | 603420183 |
Company Name | LSI Solutions, 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 | true |
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 |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Lumen/Inner Diameter | 30 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Outer Diameter | 30 Millimeter |
Outer Diameter | 35 Millimeter |
Outer Diameter | 40 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850200006261 [Primary] |
HEW | Culdoscope (And Accessories) |
LKF | Cannula, manipulator/injector, uterine |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-12-07 |
Device Publish Date | 2016-09-23 |
00850200006391 | Set of 4 FS® SOUNDS 6 cm, 8 cm, 10 cm, and 12 cm Base Package Type - Kit One (1) each non-steri |
00850200006384 | 12 cm FS® SOUND Base Package Type - Each One (1) non-sterile, reusable 12 cm FS® SOUND for use |
00850200006377 | 10 cm FS® SOUND Base Package Type - Each One (1) non-sterile, reusable 10 cm FS® SOUND for use |
00850200006360 | 8 cm FS® SOUND Base Package Type - Each One (1) non-sterile, reusable 8 cm FS® SOUND for use w |
00850200006322 | 6 cm FS® SOUND Base Package Type - Each One (1) non-sterile, reusable 6 cm FS® SOUND for use w |
00850200006261 | Combo Box of 6 FS FORNISEE® DEVICES Base Package Type - Kit The combo box contains two (2) each |
10850200006237 | FS-40 FORNISEE® DEVICE Base Package Type - Each Each sterile package contains (1) single patien |
10850200006220 | FS-35 FORNISEE® DEVICE Base Package Type - Each Each sterile package contains (1) single patien |
10850200006213 | FS-30 FORNISEE® DEVICE Base Package Type - Each Each sterile package contains (1) single patien |