Primary Device ID | 00850031859104 |
NIH Device Record Key | 79e74538-ee64-4cbc-8aea-7ca318b8e1d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aliya Generator-Recertified |
Version Model Number | GTI-00017R |
Company DUNS | 070000990 |
Company Name | Galvanize Therapeutics, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850031859104 [Primary] |
OAB | Low Energy Direct Current Thermal Ablation System |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-03-10 |
Device Publish Date | 2025-02-28 |
00850031859074 - INUMI Flex Needle | 2025-03-10 INUMI Flex Needle, 5 pack |
00850031859104 - Aliya Generator-Recertified | 2025-03-10Aliya Generator - recertified |
00850031859104 - Aliya Generator-Recertified | 2025-03-10 Aliya Generator - recertified |
00850031859043 - Aliya Generator | 2025-03-03 Aliya Generator, 2.5 |
10850031859002 - Aliya Needle | 2024-02-29 Aliya Needle, 5 pack |
10850031859026 - Aliya Electrode | 2024-02-29 Aliya Electrode, 5 pack |
00850031859050 - Aliya Generator | 2023-08-28 Aliya Generator, 2.5 |