Primary Device ID | 08800053084734 |
NIH Device Record Key | a3023a1b-79a5-4755-90a7-0eb3f1e1f5d1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SAVE Wide Cap |
Version Model Number | DSWCC700410 |
Company DUNS | 694721181 |
Company Name | DENTIS 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
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 | 08800053084734 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-08-18 |
Device Publish Date | 2023-08-10 |
08800053084710 | SAVE Wide Cap (DSWCC700208) |
08800053084703 | SAVE Wide Cap (DSWCC600410) |
08800053084697 | SAVE Wide Cap (DSWCC600309) |
08800053084680 | SAVE Wide Cap (DSWCC600208) |
08800053084765 | SAVE Wide Cap (DSWCC800410) |
08800053084758 | SAVE Wide Cap (DSWCC800309) |
08800053084741 | SAVE Wide Cap (DSWCC800208) |
08800053084734 | SAVE Wide Cap (DSWCC700410) |
08800053084727 | SAVE Wide Cap (DSWCC700309) |