Primary Device ID | 10813150020098 |
NIH Device Record Key | b34677ff-6f63-4265-a167-8cdb8ec83b76 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vermed DEFIB PADS |
Version Model Number | D310 |
Catalog Number | D310 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00813150020091 [Unit of Use] |
GS1 | 10813150020098 [Primary] |
GS1 | 20813150020095 [Package] Package: [10 Units] 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 | 2023-02-20 |
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 |