Primary Device ID | 08800070214039 |
NIH Device Record Key | 35af9d82-236b-40e9-a33d-256b4a83c4b1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Angled Abutment |
Version Model Number | AASRB52252 |
Company DUNS | 694625347 |
Company Name | Izenimplant Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 08800070214039 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08800070214039]
Moist Heat or Steam Sterilization
[08800070214039]
Moist Heat or Steam Sterilization
[08800070214039]
Moist Heat or Steam Sterilization
[08800070214039]
Moist Heat or Steam Sterilization
[08800070214039]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-26 |
Device Publish Date | 2022-05-18 |