Primary Device ID | 20726893111183 |
NIH Device Record Key | 447822a8-4b4c-4d6b-b024-ce9416d97ff9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ONE Pleasure Dome |
Version Model Number | 11200C |
Company DUNS | 364614362 |
Company Name | GLOBAL PROTECTION CORP. |
Device Count | 1 |
DM Exempt | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 20726893111183 [Primary] |
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 | 2019-09-16 |
Device Publish Date | 2019-09-08 |
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