Primary Device ID | H6680921328S1 |
NIH Device Record Key | d839008e-c228-441b-b799-095a0333bc65 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bosworth Aegis |
Version Model Number | 0921328S |
Catalog Number | 0921328S |
Company DUNS | 014769301 |
Company Name | Harry J Bosworth Company |
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 |
Phone | +1(800)333-3131 |
tschwear@keystoneind.com |
Total Volume | 0.4 Milliliter |
Storage Environment Temperature | Between 32 Degrees Fahrenheit and 86 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
HIBCC | H6680921328S1 [Primary] |
EBC | SEALANT, PIT AND FISSURE, AND CONDITIONER |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-15 |
H66809213481 | Aegis Pit & Fissure Sealant w/ACP Standard Kit |
H6680921328S1 | Aegis Pit & Fissure Sealant w/ACP 0.4 mL Sample |
H66809213281 | Aegis Pit & Fissure Sealant w/ACP Refill Kit |
H66809213271 | Aegis Pit & Fissure Sealant w/ACP Clinic Kit |