Primary Device ID | 20813150020194 |
NIH Device Record Key | 2b95291d-5a87-4691-9fbe-4bd039152382 |
Commercial Distribution Discontinuation | 2019-12-12 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Vermed DEFIB PADS |
Version Model Number | D315 |
Catalog Number | D315 |
Company DUNS | 002111896 |
Company Name | GRAPHIC CONTROLS ACQUISITION CORP |
Device Count | 10 |
DM Exempt | false |
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 | 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 | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com | |
Phone | 1.800.669.6905 |
customerservice@vermed.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813150020190 [Unit of Use] |
GS1 | 10813150020197 [Primary] |
GS1 | 20813150020194 [Package] Contains: 10813150020197 Package: [10 Units] Discontinued: 2019-12-12 Not in Commercial Distribution |
MKJ | Automated External Defibrillators (Non-Wearable) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-12-13 |
Device Publish Date | 2017-01-13 |
20813150020194 | 1 PER PACK 10 PERCASE |
10813150020074 | 1 PER PACK 10 PERCASE |
10813150020036 | 1 PER PACK 10 PERCASE |
10813150020012 | 1 PER PACK 10 PERCASE |
20813150020316 | 1 PER PACK 10 PERCASE PEDIATRIC |
20813150020293 | 1 PER PACK 10 PERCASE PEDIATRIC |
20813150020279 | 1 PER PACK 10 PERCASE PEDIATRIC |
20813150020255 | 1 PER PACK 10 PERCASEPEDIATRIC |
20813150020231 | 1 PER PACK 10 PERCASE |
20813150020217 | 1 PER PACK 10 PERCASE |
20813150020170 | 1 PER PACK 10 PERCASE |
10813150020159 | 1 PER PACK 10 PERCASE |
10813150020135 | 1 PER PACK 10 PERCASE |
10813150020111 | 1 PER PACK 10 PERCASE |
10813150020098 | 1 PER PACK 10 PERCASE |
20813150020057 | 1 PER PACK 10 PERCASE |