Primary Device ID | 00049696869737 |
NIH Device Record Key | a7fb8deb-3b83-4048-be3f-fbc32b92d009 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | 64431321 |
Company DUNS | 656091279 |
Company Name | FOURSTAR GROUP INC. |
Device Count | 1 |
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 | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00049696869737 [Primary] |
OMW | Adhesive Backed Thermal Skin Patches |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-02-13 |
Device Publish Date | 2023-02-05 |
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