Primary Device ID | 00861680000465 |
NIH Device Record Key | 48c95939-9eed-4aff-a5f8-cc46dfc2ce50 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Navina Inserts |
Version Model Number | 69302 |
Catalog Number | 69302 |
Company DUNS | 967228474 |
Company Name | RENEW MEDICAL INC |
Device Count | 30 |
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 | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 1-888-987-2929 |
ricky@renew-medical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00861680000465 [Primary] |
GS1 | 00861680000489 [Unit of Use] |
PBP | Rectal Insert |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-02-18 |
Device Publish Date | 2019-01-18 |
00861680000472 | 30 pack carton of individually packaged Navina large size single shot Inserts |
00861680000465 | 30 pack carton of individually packaged Navina regular size single shot Inserts |
00861680000458 | Starter Pack of 5 individually packaged Navina Inserts consisting of 3 regular size and 2 large |