Primary Device ID | 80726893114735 |
NIH Device Record Key | 4f049611-5ef6-4016-81c1-b6deb8b504f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ONE Super Sensitive |
Version Model Number | 1160B2C |
Company DUNS | 364614362 |
Company Name | GLOBAL PROTECTION CORP. |
Device Count | 12 |
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 | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature in a dark, dry place. Avoid excessive heat. |
Special Storage Condition, Specify | Between 0 and 0 *Store at room temperature in a dark, dry place. Avoid excessive heat. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20726893114733 [Primary] |
GS1 | 80726893114735 [Unit of Use] |
HIS | Condom |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-09-04 |
Device Publish Date | 2023-08-25 |
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