Primary Device ID | 08809262955439 |
NIH Device Record Key | 555c85ad-1f50-46f9-93be-5aff9b190409 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EsBond Activator |
Version Model Number | 101-0502 |
Catalog Number | 101-0502 |
Company DUNS | 689370711 |
Company Name | Spident Co., Ltd. |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00202201110056 [Package] Package: [12 Units] In Commercial Distribution |
GS1 | 08809262955439 [Primary] |
GS1 | 20210105170056 [Package] Package: [5 Units] In Commercial Distribution |
EBF | Material, Tooth Shade, Resin |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-05-17 |
Device Publish Date | 2018-08-21 |
08809262950007 - EsFlow PLUS | 2025-08-08 EsFlow PLUS A1 2.5g x 2sy |
08809262950014 - EsFlow PLUS | 2025-08-08 EsFlow PLUS A2 2.5g x 2sy |
08809262950021 - EsFlow PLUS | 2025-08-08 EsFlow PLUS A3 2.5g x 2sy |
08809262950038 - EsFlow PLUS | 2025-08-08 EsFlow PLUS A3.5 2.5g x 2sy |
08809262950045 - EsFlow PLUS | 2025-08-08 EsFlow PLUS B1 2.5g x 2sy |
08809262950052 - EsFlow PLUS | 2025-08-08 EsFlow PLUS B2 2.5g x 2sy |
08809262950069 - EsFlow PLUS | 2025-08-08 EsFlow PLUS AO 2.5g x 2sy |
08809262950076 - EsFlow PLUS | 2025-08-08 EsFlow PLUS AE 2.5g x 2sy |