Primary Device ID | 80070907692574 |
NIH Device Record Key | c86d11f6-fdcd-4b15-9fa6-f37ac7d9ec1a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CONTEMPO |
Version Model Number | 0068 |
Company DUNS | 672044515 |
Company Name | SURETEX LIMITED - BRANCH |
Device Count | 8 |
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 | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00070907200681 [Primary] |
GS1 | 80070907692574 [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 | 2020-09-03 |
Device Publish Date | 2020-08-26 |
80070907695186 | CONTEMPO BARE RIDER 8CT |
80070907695148 | CONTEMPO ROUGH RIDER 8CT |
80070907692574 | CONTEMPO HOT RIDER |