Primary Device ID | 10607915138490 |
NIH Device Record Key | deb1c0e6-6dfe-4460-8a52-5647c14723b6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GelPOINT V-Path |
Version Model Number | C2A15 |
Company DUNS | 187129135 |
Company Name | APPLIED MEDICAL RESOURCES CORPORATION |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com | |
Phone | 1-949-713-8300 |
contact@appliedmedical.com |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00607915138493 [Primary] |
GS1 | 10607915138490 [Package] Contains: 00607915138493 Package: [1 Units] In Commercial Distribution |
GS1 | 10607915140516 [Package] Contains: 00607915138493 Package: [1 Units] In Commercial Distribution |
GS1 | 10607915145658 [Package] Contains: 00607915138493 Package: [1 Units] In Commercial Distribution |
HEW | Culdoscope (And Accessories) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-12-20 |
Device Publish Date | 2019-09-17 |
10607915138667 | Transvaginal Access Platform |
10607915138490 | Transvaginal Access Platform |
10607915138483 | Transvaginal Access Platform |
00607915145613 | Transvaginal Access Platform |
10607915146693 | Transvaginal Access Platform with Insufflation Stabilization System |
10607915145368 | Transvaginal Access Platform with Total vNOTES Access System |
10607915145351 | Transvaginal Access Platform with Total vNOTES Access System |
10607915145344 | Transvaginal Access Platform with Total vNOTES Access System |
10607915145337 | Transvaginal Access Platform with Insufflation Stabilization System |
10607915145320 | Transvaginal Access Platform with Insufflation Stabilization System |
10607915145313 | Transvaginal Access Platform with Insufflation Stabilization System |