Primary Device ID | 17540208000469 |
NIH Device Record Key | f2195ccb-6591-42f8-9e5a-1c8eeee29191 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Select Sil Medium Body |
Version Model Number | SEL-SIL-MB-SHFS-PNK5 |
Catalog Number | SEL-SIL-MB-SHFS-PNK5 |
Company DUNS | 486717338 |
Company Name | Zendo Direct AG |
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 |
Special Storage Condition, Specify | Between 0 and 0 *Storage temperature: max. 77°F (25°C) |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07540208000462 [Primary] |
GS1 | 17540208000469 [Package] Contains: 07540208000462 Package: Carton [2 Units] In Commercial Distribution |
ELW | Material, Impression |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-08-09 |
17540208000469 | Super hydrophilic correction impression material based on addition curing vinyl silicones - Medi |
17540208000223 | Super hydrophilic correction impression material based on addition curing vinyl silicones - Medi |