Primary Device ID | 00851913006401 |
NIH Device Record Key | b1db5038-9c8d-4c0a-a608-7ce08f65d93d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PALS X |
Version Model Number | PX2020 |
Company DUNS | 150959401 |
Company Name | AXELGAARD MANUFACTURING CO., LTD. |
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 | false |
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 | false |
OTC Over-The-Counter | true |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com | |
Phone | 760-451-8000 |
support@axelgaard.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851913006401 [Primary] |
GXY | Electrode, Cutaneous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-20 |
Device Publish Date | 2024-12-12 |
00851913006418 | PALS X 2" x 4" rectangle |
00851913006401 | PALS X 2" x 2" square |