Primary Device ID | 00856509002812 |
NIH Device Record Key | 696f8cfc-32e5-41ee-9aba-b4aacb26d997 |
Commercial Distribution Discontinuation | 2019-11-07 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | RegenPerio Dental Beta-TCP |
Version Model Number | 04-005-01-RGP |
Catalog Number | 04-005-01-RGP |
Company DUNS | 024222105 |
Company Name | CYTOPHIL, INC. |
Device Count | 1 |
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 |
Total Volume | 0.5 Milliliter |
Storage Environment Temperature | Between 15 Degrees Celsius and 32 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00856509002812 [Primary] |
LYC | Bone Grafting Material, Synthetic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-10-30 |
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