Primary Device ID | 10810000526854 |
NIH Device Record Key | f99dbb02-53ce-491c-9469-02cea936017b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Retrieve™ |
Version Model Number | S292 |
Catalog Number | S292 |
Company DUNS | 009900424 |
Company Name | PARKELL, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810000526857 [Unit of Use] |
GS1 | 10810000526854 [Primary] |
EMA | Cement, Dental |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-06-03 |
Device Publish Date | 2018-09-21 |
M595S2500 | Retrieve™ Non-Eugenol Resin-Based Implant Cement |
00810000525324 | Retrieve™ DC Non-Eugenol Resin-Based Implant Cement |
00810000525621 | Retrieve™ DC Non-Eugenol Resin-Based Implant Cement (Korea) |
10810000526854 | Mixing Tip with Brown Base for E.T.C.™ & Retrieve™ (Pkg. of 30 pcs.) |