Primary Device ID | 18437016482558 |
NIH Device Record Key | 9b94e78d-a82e-4b01-a3b3-bc6433b047c3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AGUPUNT APS |
Version Model Number | A1012P |
Company DUNS | 476185710 |
Company Name | AGU PUNT SL |
Device Count | 100 |
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 | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08437016482551 [Primary] |
GS1 | 18437016482558 [Unit of Use] |
MQX | Needle, Acupuncture, Single Use |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-05 |
Device Publish Date | 2022-04-27 |
18437016482640 | Physiotherapy needles |
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18437016482404 | Physiotherapy needles |