Primary Device ID | D080XXBTCX17LXXXXX0 |
NIH Device Record Key | 0f13441c-e69e-4e48-8e20-7a831dd0ba46 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BASIS TWIN CURE |
Version Model Number | 17L |
Company DUNS | 693430001 |
Company Name | YAMAHACHI DENTAL MFG.,CO. |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | D080XXBTCX17LXXXXX0 [Primary] |
EBI | Resin, Denture, Relining, Repairing, Rebasing |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-10 |
Device Publish Date | 2023-10-02 |
04582275711127 | 1kg, V PINK |
04582275711066 | 1kg, O PINK |
04582275711035 | 1kg, LF PINK |
04582275711028 | 500ml |
04582594040830 | 40g, O PINK |
D080XXBTCX40GXXOPN0 | 40G,O PINK |
D080XXBTCX1KGXXVPN0 | 1KG,V PINK |
D080XXBTCX1KGXXOPN0 | 1KG,O PINK |
D080XXBTCX1KGXXLFP0 | 1KG,LF PINK |
D080XXBTC500MXXXXX0 | 500ML |
D080XXBTCX40GXXVPN0 | 40G,V PINK |
D080XXBTCX40GXXLFP0 | 40G,LF PINK |
D080XXBTCX40GXXLFA0 | 40G,LF α |
D080XXBTCX1KGXXLFA0 | 1KG,LF α |
D080XXBTCX17LXXXXX0 | 17L |
D080XXBTC4020XXVPN0 | 40G*20ML,V PINK |
D080XXBTC4020XXOPN0 | 40G*20ML,O PINK |
D080XXBTC4020XXLFP0 | 40G*20ML,LF PINK |
D080XXBTC4020XXLFA0 | 40G*20ML,LF α |
D080XXBTC20MLXXXXX0 | 20ML |